Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Early-onset Myopathy, Areflexia, Respiratory Distress And Dysphagia[original query] |
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Identification of a novel mutation and genotype-phenotype relationship in MEGF10 myopathy. Neuromuscular disorders : NMD 2022 4 32 (5): 436-440. Fujii Kanako, Hirano Makito, Terayama Atsushi, Inada Rino, Saito Yoshihiko, Nishino Ichizo, Nagai Yoshita |
- Page last reviewed:Feb 1, 2024
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