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Volumn 130 A, Issue 1, 2004, Pages 3-7

Memorial lecture - Hereditary sensory defects: From genes to pathogenesis

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 26; CONNEXIN 30;

EID: 4344699075     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30054     Document Type: Conference Paper
Times cited : (9)

References (17)
  • 5
    • 0027021440 scopus 로고
    • Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome
    • del Castillo I, Cohen-Salmon M, Blanchard S, Lutfalla G, Petit C. 1992. Structure of the X-linked Kallmann syndrome gene and its homologous pseudogene on the Y chromosome. Nat Genet 2:305-310.
    • (1992) Nat Genet , vol.2 , pp. 305-310
    • Del Castillo, I.1    Cohen-Salmon, M.2    Blanchard, S.3    Lutfalla, G.4    Petit, C.5
  • 8
    • 0034284683 scopus 로고    scopus 로고
    • Mariner is defective in myosin VIIA: A zebrafish model for human hereditary deafness
    • Ernest S, Rauch GJ, Haffter P, Geisler R, Petit C, Nicolson T. 2000. Mariner is defective in myosin VIIA: A zebrafish model for human hereditary deafness. Hum Mol Genet 9:2189-2196.
    • (2000) Hum Mol Genet , vol.9 , pp. 2189-2196
    • Ernest, S.1    Rauch, G.J.2    Haffter, P.3    Geisler, R.4    Petit, C.5    Nicolson, T.6
  • 10
  • 11
    • 0028306509 scopus 로고
    • A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
    • Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Welssenbach J, Drira M, Petit C. 1994b. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum Mol Genet 3:989-993.
    • (1994) Hum Mol Genet , vol.3 , pp. 989-993
    • Guilford, P.1    Ayadi, H.2    Blanchard, S.3    Chaib, H.4    Le Paslier, D.5    Welssenbach, J.6    Drira, M.7    Petit, C.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.