Clinical and genetic heterogeneity in nemaline myopathy - A disease of skeletal muscle thin filaments

Trends in Molecular Medicine

Volumn 7, Issue 8, 2001, Pages 362-368

  Sanoudou, Despina ^a   Beggs, Alan H ^b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE CLASSIFICATION; DISEASE SEVERITY; HUMAN; MUSCLE BIOPSY; MUSCLE DISEASE; MYOPATHY; NEMALINE MYOPATHY; REVIEW; SKELETAL MUSCLE; THIN FILAMENT;

EID: 0034906020     PISSN: 14714914     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1471-4914(01)02089-5     Document Type: Review

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