Congenital muscular dystrophy with primary laminin α2 (merosin) deficiency presenting as inflammatory myopathy.

Autor: Pegoraro, Elena, Cianno, Brad Di, Hoffman, Eric P., Mancias, Pedro, Swerdlow, Steven H., Raikow, Radmila B., Garcia, Carlos, Marks, Harold, Crawford, Thomas, Carver, Virginia
Zdroj: Annals of Neurology; 1996, Vol. 40 Issue 5, p782-791, 10p
Databáze: Complementary Index
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