Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
Jennifer L. Dawkins(University of Sydney), D J Hulme(Concord Repatriation General Hospital), Sonal Brahmbhatt(Anzac Research Institute), Michaela Auer‐Grumbach(University of Graz), Garth A. Nicholson(Concord Repatriation General Hospital)
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