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Volumn 75, Issue 6, 2009, Pages 572-575

Novel POU3F4 mutations and clinical features of DFN3 patients with cochlear implants

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR POU3F4; UNCLASSIFIED DRUG;

EID: 66549084555     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2009.01181.x     Document Type: Letter
Times cited : (39)

References (7)
  • 1
    • 0028988233 scopus 로고
    • Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
    • de Kok YJ, van der Maarel SM, Bitner-Glindzicz M et al. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 1995: 267: 685-688.
    • (1995) Science , vol.267 , pp. 685-688
    • de Kok, Y.J.1    van der Maarel, S.M.2    Bitner-Glindzicz, M.3
  • 3
    • 0026632820 scopus 로고
    • Brain 4: A novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression
    • Mathis JM, Simmons DM, He X et al. Brain 4: A novel mammalian POU domain transcription factor exhibiting restricted brain-specific expression. EMBO J 1992: 11: 2551-2561.
    • (1992) EMBO J , vol.11 , pp. 2551-2561
    • Mathis, J.M.1    Simmons, D.M.2    He, X.3
  • 4
    • 29144469466 scopus 로고    scopus 로고
    • Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness
    • Vore AP, Chang EH, Hoppe JE et al. Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafness. Arch Otolaryngol Head Neck Surg 2005: 131: 1057-1063.
    • (2005) Arch Otolaryngol Head Neck Surg , vol.131 , pp. 1057-1063
    • Vore, A.P.1    Chang, E.H.2    Hoppe, J.E.3
  • 5
    • 33745247186 scopus 로고    scopus 로고
    • A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family
    • Wang QJ, Li QZ, Rao SQ et al. A novel mutation of POU3F4 causes congenital profound sensorineural hearing loss in a large Chinese family. Laryngoscope 2006: 116: 944-950.
    • (2006) Laryngoscope , vol.116 , pp. 944-950
    • Wang, Q.J.1    Li, Q.Z.2    Rao, S.Q.3
  • 6
    • 0031662883 scopus 로고    scopus 로고
    • A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3)
    • Hagiwara H, Tamagawa Y, Kitamura K et al. A new mutation in the POU3F4 gene in a Japanese family with X-linked mixed deafness (DFN3). Laryngoscope 1998: 108: 1544-1547.
    • (1998) Laryngoscope , vol.108 , pp. 1544-1547
    • Hagiwara, H.1    Tamagawa, Y.2    Kitamura, K.3
  • 7
    • 0025870974 scopus 로고
    • X-linked deafness, stapes gushers and a distinctive defect of the inner ear
    • Phelps PD, Reardon W, Pembrey M et al. X-linked deafness, stapes gushers and a distinctive defect of the inner ear. Neuroradiology 1991: 33: 326-330.
    • (1991) Neuroradiology , vol.33 , pp. 326-330
    • Phelps, P.D.1    Reardon, W.2    Pembrey, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.