Hyaline Fibromatosis Syndrome: A Novel Mutation and Recurrent Founder Mutation in the CMG2/ANTXR2 Gene

被引：9
作者：
Youssefian, Leila [1 ,2 ]
Vahidnezhad, Hassan [1 ,3 ]
Aghighi, Yahya [4 ]
Ziaee, Vahid [4 ,5 ]
Zeinali, Sirous [3 ,6 ]
Abiri, Maryam [2 ,3 ]
Uitto, Jouni [1 ,2 ]
机构：
[1] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Dermatol & Cutaneous Biol, 233 S 10th St,Suite 450 BLSB, Philadelphia, PA 19107 USA
[2] Univ Tehran Med Sci, Dept Med Genet, Tehran, Iran
[3] Pasteur Inst Iran, Biotechnol Res Inst, Dept Mol Med, Tehran, Iran
[4] Tehran Univ Medial Sci, Imam Khomeini Hosp, Dept Pediat, Tehran, Iran
[5] Univ Tehran Med Sci, Rheumatol Res Ctr, Sch Med, Tehran, Iran
[6] Kawsar Human Genet Res Ctr, Tehran, Iran
来源：
ACTA DERMATO-VENEREOLOGICA | 2017年 / 97卷 / 01期
关键词：
INFANTILE SYSTEMIC HYALINOSIS; CAPILLARY MORPHOGENESIS;
D O I：
10.2340/00015555-2459
中图分类号：
R75 [皮肤病学与性病学];
学科分类号：
100206 ;
摘要：
引用
收藏
页码：108 / 109
页数：2
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