Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modeling

Nicolas Guex, Manuel C. Peitsch · Electrophoresis · 1997 · 11.3K citations

Life Sciences, Biochemistry, Bioinformatics +7

α-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere

Ludwig Thierfelder, Hugh Watkins, Calum A. MacRae et al. · Cell · 1994 · 1K citations

Medicine, Genetics, Molecular Genetics +10

Emery and Rimoin's Principles and Practice of Medical Genetics

C. Geoffrey Woods · Journal of Medical Genetics · 1997 · 714 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

NEMALINE MYOPATHY

G. MILTON SHY, W. King Engel, Jeffrey T. Somers et al. · Brain · 1963 · 469 citations

Life Sciences, Biochemistry, Physiology +16

Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

Duangrurdee Wattanasirichaigoon, Hans H. Goebel, Matthew C. J. Wilce et al. · Nature Genetics · 1999 · 401 citations

Medicine, Genetics, Molecular Genetics +13