Human genes for nemaline myopathy 9
Nemaline myopathy 9 [DOID:0110929]
A nemaline myopathy characterized by onset in early infancy of muscle weakness with variable severity that has_material_basis_in homozygous or compound heterozygous mutation in the KLHL41 gene on chromosome 2q31.
Synonyms: nemaline myopathy 9, DOID:0110929, NEM9