## Communicated by Michel Goossens Hypertrophic cardiomyopathy (HCM) is a heterogeneous autosomal dominant cardiac disorder with a prevalence of 1 in 500. Over 450 different pathogenic mutations in at least 16 genes have been identified so far. The large allelic and genetic heterogeneity of HCM r
✦ LIBER ✦
Contractures and hypertrophic cardiomyopathy in a novel FHL1 mutation
✍ Scribed by Hans Knoblauch; Christian Geier; Stephanie Adams; Birgit Budde; André Rudolph; Ute Zacharias; Jeannette Schulz-Menger; Andreas Spuler; Rabah Ben Yaou; Peter Nürnberg; Thomas Voit; Gisele Bonne; Simone Spuler
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 676 KB
- Volume
- 67
- Category
- Article
- ISSN
- 0364-5134
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
A DNA resequencing array for pathogenic
✍
Siv Fokstuen; Robert Lyle; Analia Munoz; Corinne Gehrig; René Lerch; Andreas Per
📂
Article
📅
2008
🏛
John Wiley and Sons
🌐
English
⚖ 227 KB
First mutation in cardiac troponin C, L2
✍
Bernard Hoffmann; Hajo Schmidt-Traub; Andreas Perrot; Karl Josef Osterziel; Rein
📂
Article
📅
2001
🏛
John Wiley and Sons
🌐
English
⚖ 15 KB
Hypertrophic cardiomyopathy in a girl wi
✍
Giuseppe Limongelli; Silvia Russo; Maria Cristina Digilio; Maura Masciadri; Gius
📂
Article
📅
2010
🏛
John Wiley and Sons
🌐
English
⚖ 149 KB
👁 2 views
Apical hypertrophic cardiomyopathy in a
✍
Malouf, Joe ;Ratl, Habib ;Der Kaloustian, Vazken M. ;Opitz, John M. ;Reynolds, J
📂
Article
📅
1985
🏛
John Wiley and Sons
🌐
English
⚖ 446 KB
👁 1 views
Implantable cardioverter defibrillator f
✍
Yasushi Wakabayashi; Kyohei Yamazaki; Yoko Narumi; Satoshi Fuseya; Miki Horigome
📂
Article
📅
2011
🏛
John Wiley and Sons
🌐
English
⚖ 168 KB
👁 1 views
A rapid protocol for cardiac troponin T
✍
Brenda Gerull; Karl-Josef Osterziel; Christian Witt; Rainer Dietz; Ludwig Thierf
📂
Article
📅
1998
🏛
John Wiley and Sons
🌐
English
⚖ 143 KB
Mutations in the human cardiac troponin T gene (TNNT2) are associated with familial hypertrophic cardiomyopathy (FHC) linked to chromosome 1q3 (CMH2). Mutation analyses of TNNT2 have been restricted to RNA-based screening methods because only the TNNT2 cDNA sequence was known. We characterized the g