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Volumn 253, Issue 9, 2006, Pages 1234-1235

GDAP1 mutation in autosomal recessive Charcot-Marie-Tooth with pyramidal features [4]

Author keywords

[No Author keywords available]

Indexed keywords

GANGLIOSIDE INDUCED DIFFERENTIATION ASSOCIATED PROTEIN 1; PROTEIN; UNCLASSIFIED DRUG;

EID: 33749446331     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-006-0149-4     Document Type: Letter
Times cited : (9)

References (8)
  • 6
    • 17744376804 scopus 로고    scopus 로고
    • GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria
    • Pedrola L, Espert A, Wu X, Claramunt R, Shy ME, Palau F. (2005). GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria. Hum Mol Genet 14:1087-1094
    • (2005) Hum Mol Genet , vol.14 , pp. 1087-1094
    • Pedrola, L.1    Espert, A.2    Wu, X.3    Claramunt, R.4    Shy, M.E.5    Palau, F.6
  • 8
    • 23244443545 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: Families with and without MFN2 mutations
    • Zhu D, Kennerson ML, Walizada G, Zuchner S, Vance JM, Nicholson GA. (2005). Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations. Neurology 65:496-497
    • (2005) Neurology , vol.65 , pp. 496-497
    • Zhu, D.1    Kennerson, M.L.2    Walizada, G.3    Zuchner, S.4    Vance, J.M.5    Nicholson, G.A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.