APA

Pegoraro E., Mancias P., Swerdlow S. H., Raikow R. B., Garcia C., Marks H., Crawford T., Carver V., Di Cianno B. & Hoffman E. P. (19970123). Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. : Annals of neurology.

Chicago

Pegoraro E, Mancias P, Swerdlow S H, Raikow R B, Garcia C, Marks H, Crawford T, Carver V, Di Cianno B and Hoffman E P. 19970123. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. : Annals of neurology.

Harvard

Pegoraro E., Mancias P., Swerdlow S. H., Raikow R. B., Garcia C., Marks H., Crawford T., Carver V., Di Cianno B. and Hoffman E. P. (19970123). Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. : Annals of neurology.

MLA

Pegoraro E, Mancias P, Swerdlow S H, Raikow R B, Garcia C, Marks H, Crawford T, Carver V, Di Cianno B and Hoffman E P. Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy. : Annals of neurology. 19970123.