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
收藏
页码：G21 / G21
页数：1
相关论文
共 50 条
[41]   A MOLECULAR-BASIS FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - AN ALPHA-BETA-CARDIAC MYOSIN HEAVY-CHAIN HYBRID GENE [J].
TANIGAWA, G ;
JARCHO, JA ;
KASS, S ;
SOLOMON, SD ;
VOSBERG, HP ;
SEIDMAN, JG ;
SEIDMAN, CE .
CELL, 1990, 62 (05) :991-998
[42]   β-myosin heavy chain gene mutations in familial hypertrophic cardiomyopathy -: The usual suspect? [J].
McNally, EM .
CIRCULATION RESEARCH, 2002, 90 (03) :246-247
[43]   The pathogenesis of familial hypertrophic cardiomyopathy: Early and evolving effects from an α-cardiac myosin heavy chain missense mutation [J].
Dimitrios Georgakopoulos ;
Michael E. Christe ;
Michael Giewat ;
Christine M. Seidman ;
J.G. Seidman ;
David A. Kass .
Nature Medicine, 1999, 5 :327-330
[44]   The pathogenesis of familial hypertrophic cardiomyopathy:: Early and evolving effects from an α-cardiac myosin heavy chain missense mutation [J].
Georgakopoulos, D ;
Christe, ME ;
Giewat, M ;
Seidman, CM ;
Seidman, JG ;
Kass, DA .
NATURE MEDICINE, 1999, 5 (03) :327-330
[45]   DETECTION OF A NEW MUTATION IN THE BETA-MYOSIN HEAVY-CHAIN GENE IN AN INDIVIDUAL WITH HYPERTROPHIC CARDIOMYOPATHY [J].
MARIAN, AJ ;
YU, QT ;
MARES, A ;
HILL, R ;
ROBERTS, R ;
PERRYMAN, MB .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) :2156-2165
[46]   A previously undescribed de novo insertion-deletion mutation in the beta myosin heavy chain gene in a kindred with familial hypertrophic cardiomyopathy [J].
Cuda, G ;
Perrotti, N ;
Perticone, F ;
Mattioli, PL .
HEART, 1996, 76 (05) :451-452
[47]   A NEW MUTATION OF CARDIAC MYOSIN HEAVY-CHAIN GENE IN A ITALIAN FAMILY WITH HYPERTROPHIC CARDIOMYOPATHY (FHC) [J].
COVIELLO, DA ;
SPIRITO, P ;
TROJANI, A ;
BERTORELLI, R ;
PANUCCI, E ;
AUTORE, C ;
VECCHIO, C ;
RAVAZZOLO, R .
AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) :1724-1724
[48]   Molecular genetic screening of α-myosin heavy chain in dilated and hypertrophic cardiomyopathy. [J].
Carniel, E ;
Taylor, MRG ;
Fain, PR ;
Di Lenarda, A ;
Sinagra, G ;
Lascor, J ;
Ku, L ;
Feiger, J ;
Slavov, D ;
Zhu, X ;
Dao, D ;
Ferguson, DA ;
Mestroni, L .
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) :166-166
[49]   Familial Hypertrophic Cardiomyopathy Associated with Cardiac β-Myosin Heavy Chain and Troponin I Mutations [J].
Aisha Frazier ;
Daniel P. Judge ;
Steven P. Schulman ;
Nicole Johnson ;
Kathryn W. Holmes ;
Anne M. Murphy .
Pediatric Cardiology, 2008, 29 :846-850
[50]   MUTATIONS IN CARDIAC MYOSIN HEAVY-CHAIN GENES CAUSE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY [J].
SEIDMAN, CE ;
SEIDMAN, JG .
MOLECULAR BIOLOGY & MEDICINE, 1991, 8 (02) :159-166
12345