Lane J. Mahoney

Mutation spectrum in the large GTPase dynamin 2, and genotype-phenotype correlation in autosomal dominant centronuclear myopathy

Johann Böhm, Valérie Biancalana, Elizabeth T. DeChene et al. · Human Mutation · 2012 · 135 citations · Full text

Peripheral Neuropathy, Mendelian Disorder, Autoimmune Disease +15

Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores

Steven E. Boyden, Lane J. Mahoney, Genri Kawahara et al. · Neurogenetics · 2012 · 82 citations · Full text

Mitochondrial Myopathy, Rare Diseases, Murine Megf10 +13

Silencing of drpr Leads to Muscle and Brain Degeneration in Adult Drosophila

Isabelle Draper, Lane J. Mahoney, Satomi Mitsuhashi et al. · American Journal Of Pathology · 2014 · 24 citations · Full text

Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE

Steven E. Boyden, Anna R. Duncan, Elicia Estrella et al. · BMC Medical Genetics · 2011 · 20 citations · Full text

Homozygous nonsense mutation in<i>SGCA</i>is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt

Hemakumar M. Reddy, Sherifa A. Hamed, Monkol Lek et al. · Muscle & Nerve · 2016 · 16 citations · Full text