Syndromic congenital myelofibrosis associated with a loss-of-function variant in RBSN

被引:8
作者
Magoulas, Pilar L. [1 ,2 ]
Shchelochkov, Oleg A. [3 ]
Bainbridge, Matthew N. [4 ]
Ben-Shachar, Shay [5 ]
Yatsenko, Svetlana [6 ,7 ,8 ]
Potocki, Lorraine [1 ,2 ]
Lewis, Richard A. [2 ,9 ]
Searby, Charles [10 ]
Marcogliese, Andrea N. [1 ,11 ,12 ]
Elghetany, M. Tarek [1 ,11 ,12 ]
Zapata, Gladys [2 ,13 ]
Hernandez, Paula P. [2 ,13 ]
Gadkari, Manasi [14 ]
Einhaus, Derek [14 ]
Muzny, Donna M. [15 ]
Gibbs, Richard A. [15 ]
Bertuch, Alison A. [1 ,12 ]
Scott, Daryl A. [1 ,2 ,16 ]
Corvera, Silvia [17 ]
Franco, Luis M. [14 ]
机构
[1] Texas Childrens Hosp, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[3] NHGRI, Med Genom & Metab Genet Branch, NIH, Bethesda, MD 20892 USA
[4] Rady Childrens Inst Genom Med, San Diego, CA USA
[5] Tel Aviv Univ, Genet Inst, Tel Aviv Sourasky Med Ctr, Sackler Fac Med, Tel Aviv, Israel
[6] Univ Pittsburgh, Sch Med, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA USA
[7] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA USA
[8] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15261 USA
[9] Baylor Coll Med, Dept Ophthalmol, Houston, TX 77030 USA
[10] Univ Iowa, Iowa City, IA USA
[11] Baylor Coll Med, Dept Pathol & Immunol, Houston, TX 77030 USA
[12] Baylor Coll Med, Dept Pediat, Sect Hematol & Oncol, Houston, TX 77030 USA
[13] Baylor Coll Med, USDA ARS, Childrens Nutr Res Ctr, Sect Nutr,Dept Pediat, Houston, TX 77030 USA
[14] NIAID, Lab Immune Syst Biol, NIH, 9000 Rockville Pike,Bldg 4,Room 138, Bethesda, MD 20892 USA
[15] Baylor Coll Med, Human Genome Sequencing Ctr, Houston, TX 77030 USA
[16] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
[17] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA USA
基金
美国国家卫生研究院;
关键词
RABENOSYN-5; MUTATION; NEUTROPENIA;
D O I
10.1182/blood-2017-12-824433
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:658 / 662
页数:5
相关论文
共 50 条
  • [41] Severe post-partum autoimmune hypothyroidism associated with a novel loss-of-function mutation in intracellular domain of human thyrotropin receptor
    Bose, Arindam
    Sharma, Norman
    Hemvani, Nanda
    Chitnis, Dhananjay S.
    MEDICAL STUDIES-STUDIA MEDYCZNE, 2016, 32 (04) : 294 - 298
  • [42] Filaggrin loss-of-function mutations as a predictor for atopic eczema, allergic sensitization and eczema-associated asthma in Polish children population
    Debinska, Anna
    Danielewicz, Hanna
    Drabik-Chamerska, Anna
    Kalita, Danuta
    Boznanski, Andrzej
    ADVANCES IN CLINICAL AND EXPERIMENTAL MEDICINE, 2017, 26 (06): : 991 - 998
  • [43] Loss-of-function variants in Kv11.1 cardiac channels as a biomarker for SUDEP
    Soh, Ming S.
    Bagnall, Richard D.
    Bennett, Mark F.
    Bleakley, Lauren E.
    Mohamed Syazwan, Erlina S.
    Marie Phillips, A.
    Chiam, Mathew D. F.
    McKenzie, Chaseley E.
    Hildebrand, Michael
    Crompton, Douglas
    Bahlo, Melanie
    Semsarian, Christopher
    Scheffer, Ingrid E.
    Berkovic, Samuel F.
    Reid, Christopher A.
    ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2021, 8 (07): : 1422 - 1432
  • [44] Milder presentation of osteogenesis imperfecta type VIII due to compound heterozygosity for a predicted loss-of-function variant and novel missense variant in P3H1-further expansion of the phenotypic spectrum
    Mikhail, Kristen A.
    VanSickle, Elizabeth
    Rossetti, Linda Z.
    COLD SPRING HARBOR MOLECULAR CASE STUDIES, 2023, 9 (01):
  • [45] Loss-of-function variants in ABCA7 confer risk of Alzheimer's disease
    Steinberg, Stacy
    Stefansson, Hreinn
    Jonsson, Thorlakur
    Johannsdottir, Hrefna
    Ingason, Andres
    Helgason, Hannes
    Sulem, Patrick
    Magnusson, Olafur Th
    Gudjonsson, Sigurjon A.
    Unnsteinsdottir, Unnur
    Kong, Augustine
    Helisalmi, Seppo
    Soininen, Hilkka
    Lah, James J.
    Aarsland, Dag
    Fladby, Tormod
    Ulstein, Ingun D.
    Djurovic, Srdjan
    Sando, Sigrid B.
    White, Linda R.
    Knudsen, Gun-Peggy
    Westlye, Lars T.
    Selbaek, Geir
    Giegling, Ina
    Hampel, Harald
    Hiltunen, Mikko
    Levey, Allan I.
    Andreassen, Ole A.
    Rujescu, Dan
    Jonsson, Palmi V.
    Bjornsson, Sigurbjorn
    Snaedal, Jon
    Stefansson, Kari
    NATURE GENETICS, 2015, 47 (05) : 445 - U24
  • [46] Partial loss-of-function of sodium channel SCN8A in familial isolated myoclonus
    Wagnon, Jacy L.
    Mencacci, Niccolo E.
    Barker, Bryan S.
    Wengert, Eric R.
    Bhatia, Kailash P.
    Balint, Bettina
    Carecchio, Miryam
    Wood, Nicholas W.
    Patel, Manoj K.
    Meisler, Miriam H.
    HUMAN MUTATION, 2018, 39 (07) : 965 - 969
  • [47] Loss-of-function OGFRL1 variants identified in autosomal recessive cherubism families
    Kittaka, Mizuho
    Mizuno, Noriyoshi
    Morino, Hiroyuki
    Yoshimoto, Tetsuya
    Zhu, Tianli
    Liu, Sheng
    Wang, Ziyi
    Mayahara, Kotoe
    Iio, Kyohei
    Kondo, Kaori
    Kondo, Toshio
    Hayashi, Tatsuhide
    Coghlan, Sarah
    Teno, Yayoi
    Doan, Andrew Anh Phung
    Levitan, Marcus
    Choi, Roy B.
    Matsuda, Shinji
    Ouhara, Kazuhisa
    Wan, Jun
    Cassidy, Annelise M.
    Pelletier, Stephane
    Nampoothiri, Sheela
    Urtizberea, Andoni J.
    Robling, Alexander G.
    Ono, Mitsuaki
    Kawakami, Hideshi
    Reichenberger, Ernst J.
    Ueki, Yasuyoshi
    JBMR PLUS, 2024, 8 (06)
  • [48] Biallelic loss-of-function variations in BTD cause profound biotinidase deficiency in an Indian patient
    Kannan, Balachander
    Jayaseelan, Vijayashree Priyadharsini
    Arumugam, Paramasivam
    Navamani, Hephzibah Kirubamani
    Dv, Lal
    MOLECULAR BIOLOGY REPORTS, 2024, 51 (01)
  • [49] Mutation screening of SCN2A in schizophrenia and identification of a novel loss-of-function mutation
    Carroll, Liam S.
    Woolf, Rebecca
    Ibrahim, Yousef
    Williams, Hywel J.
    Dwyer, Sarah
    Walters, James
    Kirov, George
    O'Donovan, Michael C.
    Owen, Michael J.
    PSYCHIATRIC GENETICS, 2016, 26 (02) : 60 - 65
  • [50] Novel SCN9A variant associated with congenital insensitivity to pain
    Yammine, Tony
    Aprahamian, Raffi
    Souaid, Mirna
    Salem, Nabiha
    Awwad, Johnny
    Farra, Chantal
    MOLECULAR BIOLOGY REPORTS, 2023, 50 (07) : 6293 - 6298