Fingerprint
Dive into the research topics of 'Congenital muscular dystrophy with primary laminin α2 (Merosin) deficiency presenting as inflammatory myopathy'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
Congenital muscular dystrophy with primary laminin α2 (Merosin) deficiency presenting as inflammatory myopathy
Elena Pegoraro, Pedro Mancias, Steven H. Swerdlow, Radmila B. Raikow, Carlos Garcia, Harold Marks, Thomas Crawford, Virginia Carver, Brad Di Cianno, Eric P. Hoffman
Research output: Contribution to journal › Article › peer-review
92
Scopus
citations