Associated Papers
Intrafamilial phenotypic variations in familial cases of cervical flexion induced myelopathy/Hirayama disease.
Polavarapu K et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2018
Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy.
Lim YM et al.
Neuromuscular Disorders : Nmd, 2012
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