Genetics

DETERMINING CAUSES: Louis Kunkel believes that researching sarcoglycans will provide a better understanding of muscular dystrophy. C.G. Bonnemann, R. Modi, S. Noguchi, Y. Mizuno, M. Yoshida, E. Gussoni, E.M. McNally, D.J. Duggan, C. Angelini, E.P. Hoffman, E. Ozawa, L. Kunkel, "b-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex," Nature Genetics, 11:266-73, 1995. (Cited in 76 papers through August 1997) Comments by Louis M. Kunkel, D

Written byEugene Russo

| 3 min read

Listen with Speechify

0:00

3:00

DETERMINING CAUSES: Louis Kunkel believes that researching sarcoglycans will provide a better understanding of muscular dystrophy.

C.G. Bonnemann, R. Modi, S. Noguchi, Y. Mizuno, M. Yoshida, E. Gussoni, E.M. McNally, D.J. Duggan, C. Angelini, E.P. Hoffman, E. Ozawa, L. Kunkel, "b-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex," Nature Genetics, 11:266-73, 1995. (Cited in 76 papers through August 1997) Comments by Louis M. Kunkel, Departments of Genetics and Pediatrics and Howard Hughes Medical Institute, Harvard Medical School

L.E. Lim, F. Duclos, O. Broux, N. Bourg, Y. Sunada, V. Allamand, J. Meyer, I. Richard, C. Moomaw, C. Slaughter, F.M.S. Tome, M. Fardeau, C.E. Jackson, J.S. Beckmann, K.P. Campbell, "b-sarcoglycan: Characterization and role in limb-girdle muscular dystrophy linked to 4q12," Nature Genetics, 11:257-65, 1995. (Cited in 79 papers through August 1997) Comments by Kevin P. Campbell, Departments of Physiology, Biophysics, and Neurology and Howard Hughes Medical ...

Interested in reading more?

Become a Member of

Receive full access to digital editions of The Scientist, as well as TS Digest, feature stories, more than 35 years of archives, and much more!

Join for free today

Already a member? Login Here