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Altered TDP‐43‐dependent splicing in HSPB8‐related distal hereditary motor neuropathy and myofibrillar myopathy - Cortese - 2018 - European Journal of Neurology - Wiley Online Library
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Hereditary Neuropathy Foundation - Could you be 1 of the estimated 3300 patients in the US with the gene causing SORD Deficiency? You may have been diagnosed with CMT2, or distal hereditary
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Distal Hereditary Motor Neuronopathy Type 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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A family with distal hereditary motor neuropathy and a K141Q mutation of small heat shock protein HSPB1. | Semantic Scholar
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Frontiers | Clinical and Genetic Features of Biallelic Mutations in SORD in a Series of Chinese Patients With Charcot-Marie-Tooth and Distal Hereditary Motor Neuropathy
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Autosomal Recessive Distal Hereditary Motor Neuropathy disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
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Distal hereditary motor neuropathy with vocal cord paresis: from difficulty in choral singing to a molecular genetic diagnosis | Practical Neurology
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Figure 2 from A recurrent WARS mutation is a novel cause of autosomal dominant distal hereditary motor neuropathy | Semantic Scholar
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