De novo SPTAN1 mutation in axonal sensorimotor neuropathy and developmental disorder
- PMID: 33206935
- DOI: 10.1093/brain/awaa344
De novo SPTAN1 mutation in axonal sensorimotor neuropathy and developmental disorder
Comment in
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Reply: De novo SPTAN1 mutation in axonal sensorimotor neuropathy and developmental disorder.Brain. 2020 Dec 1;143(12):e105. doi: 10.1093/brain/awaa345. Brain. 2020. PMID: 33207363 No abstract available.
Comment on
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Nonsense mutations in alpha-II spectrin in three families with juvenile onset hereditary motor neuropathy.Brain. 2019 Sep 1;142(9):2605-2616. doi: 10.1093/brain/awz216. Brain. 2019. PMID: 31332438
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