De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III) (Q28118945)
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(P31) (Q13442814)
(P304) 266–268
(P407) (Q1860)
(P433) 3
(P478) 5
(P577) Monday, November 1, 1993
(P921) (Q15270307)
(P1433) (Q976454)
(P1476) "De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)" (language: en)
(P2093) K. Hayasaka
M. Himoro
Y. Sawaishi
K. Nanao
T. Takahashi
G. Takada
G. A. Nicholson
R. A. Ouvrier
N. Tachi
(P2860) (Q24311502)
(Q28259175)
(Q42144462)
(Q31158469)
(Q55671003)
(Q52477890)
(Q28259764)
(Q34242601)
(Q57624287)
(Q66920286)
(Q59698155)
(Q67482921)
(Q28207585)
(Q28285352)
(Q56591726)
(Q28281461)
(Q46433330)
(Q52243847)
(Q46253315)
(Q35013854)
(Q40518886)
(Q40525251)
(Q22066207)
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