Identification of a novel beta-cardiac myosin heavy chain gene mutation that causes familial hypertrophic cardiomyopathy.

被引：0

作者：

Andersen, PS

Havndrup, O

Bundgaard, H

Larsen, LA

Kanters, JK

Brandt, NJ

Vuust, J

Kjeldsen, K

Christiansen, M

机构：

[1] STATENS SERUM INST,DEPT CLIN BIOCHEM,DK-2300 COPENHAGEN,DENMARK

[2] RIGSHOSP,DEPT INTERNAL MED B,DK-2100 COPENHAGEN,DENMARK

[3] ELSINORE HOSP,DEPT INTERNAL MED,DK-3000 HELSINGOR,DENMARK

来源：

AMERICAN JOURNAL OF PATHOLOGY | 1997年 / 151卷 / 05期

关键词：

D O I：

暂无

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

引用

页码：G21 / G21

页数：1

共 50 条

[21] Impact of Human Beta-Cardiac Myosin Mutation Implicated in Both Hypertrophic and Dilated Cardiomyopathy [J].

Tang, Wanjian ;

Gunther, Laura K. ;

Cooper, Jonathan ;

Desetty, Rohini ;

Yengo, Christopher M. .

BIOPHYSICAL JOURNAL, 2019, 116 (03) :263A-264A

[22] Malalignment of the sarcomeric filaments in hypertrophic cardiomyopathy with cardiac myosin heavy chain gene mutation [J].

Muraishi, A ;

Kai, H ;

Adachi, K ;

Nishi, H ;

Imaizumi, T .

HEART, 1999, 82 (05) :625-629

[23] A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy [J].

Jaaskelainen, Pertti ;

Helio, Tiina ;

Aalto-Setala, Katriina ;

Kaartinen, Maija ;

Ilveskoski, Erkki ;

Hamalainen, Liisa ;

Melin, John ;

Karkkainen, Satu ;

Peuhkurinen, Keijo ;

Nieminen, Markku S. ;

Laakso, Markku ;

Kuusisto, Johanna .

ANNALS OF MEDICINE, 2014, 46 (06) :424-429

[24] STRUCTURAL INTERPRETATION OF THE MUTATIONS IN THE BETA-CARDIAC MYOSIN THAT HAVE BEEN IMPLICATED IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY [J].

RAYMENT, I ;

HOLDEN, HM ;

SELLERS, JR ;

FANANAPAZIR, L ;

EPSTEIN, ND .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) :3864-3868

[25] A novel mutation in the troponin I gene is associated with sudden cardiac death in familial hypertrophic cardiomyopathy. [J].

Klausen, IC ;

Mogensen, J ;

Egeblad, H ;

Baandrup, U ;

Borglum, AD .

AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) :A305-A305

[26] Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain [J].

Bundgaard, H ;

Havndrup, O ;

Andersen, PS ;

Larsen, LA ;

Brandt, NJ ;

Vuust, J ;

Kjeldsen, K ;

Christiansen, M .

JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1999, 31 (04) :745-750

[27] A β myosin heavy chain gene mutation causes restrictive cardiomyopathy [J].

Jedeikin, R ;

Bensley, M ;

Hershberger, R ;

Rice, M ;

Reijo-Pera, R ;

Sehnert, A .

PEDIATRIC RESEARCH, 2003, 53 (04) :34A-34A

[28] The possible modifier effect of a mitochondrial DNA mutation in familial hypertrophic cardiomyopathy due to beta-myosin heavy chain gene mutation [J].

Arbustini, E ;

Diegoli, M ;

Pisani, A ;

Banchieri, N ;

Repetto, A ;

Grasso, M ;

Brega, A ;

Tavazzi, L .

EUROPEAN HEART JOURNAL, 2003, 24 :562-562

[29] Phenotype comparison of familial hypertrophic cardiomyopathy with β-myosin heavy chain gene mutation with or without mitochondrial DNA mutation [J].

Arai, S ;

Joh-O, K ;

Furutani, M ;

Hayashi, J ;

Imamura, S ;

Nishikawa, T ;

Nagao, H ;

Takao, A ;

Momma, K ;

Matsuoka, R .

CIRCULATION, 1999, 100 (18) :817-817

[30] IDENTIFICATION OF ALPHA-CARDIAC AND BETA-CARDIAC MYOSIN HEAVY-CHAIN ISOFORMS AS MAJOR AUTOANTIGENS IN DILATED CARDIOMYOPATHY [J].

CAFORIO, ALP ;

GRAZZINI, M ;

MANN, JM ;

KEELING, PJ ;

BOTTAZZO, GF ;

MCKENNA, WJ ;

SCHIAFFINO, S .

CIRCULATION, 1992, 85 (05) :1734-1742

← 1 2 3 4 5 →