Myopathy, Centronuclear, Autosomal Recessive [Supplementary Concept]

mutation in amphiphysin-2

Date introduced: November 5, 2012

MeSH Unique ID: C562934

Heading Mapped to:

• Myopathies, Structural, Congenital

Entry Terms:

• Myotubular Myopathy, Autosomal Recessive