✦ LIBER ✦

Unequal allelic expression of wild-type and mutated β-myosin in familial hypertrophic cardiomyopathy

✍ Scribed by Snigdha Tripathi; Imke Schultz; Edgar Becker; Judith Montag; Bianca Borchert; Antonio Francino; Francisco Navarro-Lopez; Andreas Perrot; Cemil Özcelik; Karl-Josef Osterziel; William J. McKenna; Bernhard Brenner; Theresia Kraft

Publisher: Springer
Year: 2011
Tongue: English
Weight: 557 KB
Volume: 106
Category: Article
ISSN: 0300-8428
DOI: 10.1007/s00395-011-0205-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Functional and spectroscopic studies of

Functional and spectroscopic studies of a familial hypertrophic cardiomyopathy mutation in Motif X of cardiac myosin binding protein-C

✍ Louise J. Brown; Leena Singh; Kenneth L. Sale; Bing Yu; Ronald Trent; Peter G. F 📂 Article 📅 2002 🏛 Springer 🌐 English ⚖ 195 KB

Identification of two novel mutations in

Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy

✍ Jeanne Flavigny; Pascale Richard; Richard Isnard; Lucie Carrier; Philippe Charro 📂 Article 📅 1998 🏛 Springer 🌐 English ⚖ 434 KB

A novel missense mutation (R712L) adjace

A novel missense mutation (R712L) adjacent to the “active thiol” region of the cardiac β-myosin heavy chain gene causing hypertrophic cardiomyopathy in an Indian family

✍ Sadayappan Sakthivel; Pulavelil Kurian Joseph; Jagan Mohan Tharakan; Hans-Peter 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 13 KB 👁 3 views

A novel missense mutation (R712L) adjacent to the "active thiol" region of the cardiac ß-myosin heavy chain gene causing