Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutation.

Autosomal recessive muscular dystrophy is genetically heterogeneous. One form of this disorder, limb-girdle muscular dystrophy type 2C (LGMD 2C), is prevalent in northern Africa and has been shown to be associated with a single mutation in the gene encoding the dystrophin-associated protein gamma-sa...

Cur síos iomlán

Na minha lista:
Sonraí Bibleagrafaíochta
Main Authors: McNally, E. M., Passos-Bueno, M. R., Bönnemann, C. G., Vainzof, M., de Sá Moreira, E., Lidov, H. G., Othmane, K. B., Denton, P. H., Vance, J. M., Zatz, M., Kunkel, L. M.
Formáid: Artigo
Teanga:Inglês
Foilsithe: 1996
Ábhair:
Research Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1914841/
https://ncbi.nlm.nih.gov/pubmed/8900232
Clibeanna: Cuir Clib Leis
Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!

Míreanna Comhchosúla