Hereditary Inclusion Body Myopathy Maps to Chromosome 9p1-q1Stella Mitrani‐Rosenbaum, J G Seidman, Zohar Argov et al.|Human Molecular Genetics|1996Cited by 105
Novel Mutations Widen the Phenotypic Spectrum of Slow Skeletal/β-Cardiac Myosin (<i>MYH7</i>) Distal MyopathyPhillipa J. Lamont, Nigel G. Laing, William Wallefeld et al.|Human Mutation|2014Cited by 98
Common mutations in the phosphofructokinase-M gene in Ashkenazi Jewish patients with glycogenesis VII--and their population frequency.Jeffrey B. Sherman, Paul H. Plötz, Nina Raben et al.|PubMed|1994Cited by 66
Polymyositis: An overdiagnosed entityFrederick W. Miller, Carmine V. Oddis, Seward B. Rutkove et al.|Neurology|2004Cited by 55
Various classes of mutations in patients with phosphofructokinase deficiency (Tarui's disease)Nina Raben, Paul H. Plötz, Jeffrey B. Sherman et al.|Muscle & Nerve|1995Cited by 14