Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation (Q43168798)
scientific article published on 19 October 2005
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(P31) (Q13442814)
(Q2782326)
(P304) 527-530
(P407) (Q1860)
(P433) 6
(P478) 43
(P577) Wednesday, October 19, 2005
(P921) (Q181600)
(Q124059385)
(P1433) (Q14640281)
(P1476) "Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation" (language: en)
(P2093) M M Trudeau
J C Dalton
J W Day
L P W Ranum
M H Meisler
(P2860) (Q36216288)
(Q34388928)
(Q35993999)
(Q28291611)
(Q28212831)
(Q28207332)
(Q48470925)
(Q34432267)
(Q24533495)
(Q33945987)
(Q34142210)
(Q24653551)
(Q22253421)
(Q22010507)
(Q28141226)
(Q40831701)
(Q22008052)
(Q48601594)
(Q28314940)
(Q45269961)
(Q45245210)
(Q51934234)
(Q47843312)
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(Q48264922)
(Q43551102)
(Q77347116)
(Q56909022)
(Q81615419)
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description scientific article published on 19 October 2005

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