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Assignment of a human skeletal muscle sodium channel alpha-subunit gene (SCN4A) to 17q23.1-25.3.
David Mahoney Institute of Neurological Sciences, University of Pennsylvania School of Medicine, Philadelphia 19104.
PMID: 1851726 [PubMed - indexed for MEDLINE]
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Cited by 6 PubMed Central articles
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Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica.
Kim J, Hahn Y, Sohn EH, Lee YJ, Yun JH, Kim JM, Chung JH.
J Neurol Neurosurg Psychiatry. 2001 May; 70(5):618-23.
[J Neurol Neurosurg Psychiatry. 2001]
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Targeted gene walking by low stringency polymerase chain reaction: assignment of a putative human brain sodium channel gene (SCN3A) to chromosome 2q24-31.
Malo MS, Srivastava K, Andresen JM, Chen XN, Korenberg JR, Ingram VM.
Proc Natl Acad Sci U S A. 1994 Apr 12; 91(8):2975-9.
[Proc Natl Acad Sci U S A. 1994]
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ReviewMouse homologues of human hereditary disease.
Searle AG, Edwards JH, Hall JG.
J Med Genet. 1994 Jan; 31(1):1-19.
[J Med Genet. 1994]
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