Associated Papers
Current advance on distal myopathy genetics.
Ranta-Aho J et al.
Current Opinion in Neurology, 2024
Genomic and phenotypic landscapes of X-linked hereditary hearing loss in the Chinese population.
Feng H et al.
Orphanet Journal of Rare Diseases, 2024
Novel mutation of SMPX-related scapuloperoneal myopathy and myofibrillar myopathy.
Li Z et al.
Acta Neuropathologica, 2024
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions.
Johari M et al.
Acta Neuropathologica, 2021
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