Hereditary Inclusion Body Myopathy (HIBM) is a homozygous recessive disorder characterized by the M712T mutation. Humans who inherit this disorder develop skeletal muscle wasting, which is largely attributed to a sialic acid deficiency. In order to de . . .

Hereditary Inclusion Body Myopathy (HIBM) is a homozygous recessive disorder characterized by the M712T mutation. Humans who inherit this disorder develop skeletal muscle wasting, which is largely attributed to a sialic acid deficiency. In order to de . . .