Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss (2014)
- Authors:
- USP affiliated authors: ROSENBERG, CARLA - IB ; NETTO, REGINA CELIA MINGRONI - IB
- Unidade: IB
- DOI: 10.1016/j.ejmg.2014.02.006
- Subjects: PERDA AUDITIVA HEREDITÁRIA; GENÉTICA MÉDICA; PERDA AUDITIVA NEUROSSENSORIAL; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher place: Issy les Moulineaux
- Date published: 2014
- Source:
- Título do periódico: European Journal of Medical Genetics
- ISSN: 1769-7212
- Volume/Número/Paginação/Ano: v. 57, n. 4, p. 125-128, Mar. 2014
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
FREITAS, Erika L et al. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss. European Journal of Medical Genetics, v. 57, n. 4, p. 125-128, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.ejmg.2014.02.006. Acesso em: 16 maio 2024. -
APA
Freitas, E. L., Oiticica, J., Silva, A. G., Bittar, R. S. M., Rosenberg, C., & Mingroni Netto, R. C. (2014). Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss. European Journal of Medical Genetics, 57( 4), 125-128. doi:10.1016/j.ejmg.2014.02.006 -
NLM
Freitas EL, Oiticica J, Silva AG, Bittar RSM, Rosenberg C, Mingroni Netto RC. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss [Internet]. European Journal of Medical Genetics. 2014 ; 57( 4): 125-128.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ejmg.2014.02.006 -
Vancouver
Freitas EL, Oiticica J, Silva AG, Bittar RSM, Rosenberg C, Mingroni Netto RC. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss [Internet]. European Journal of Medical Genetics. 2014 ; 57( 4): 125-128.[citado 2024 maio 16 ] Available from: https://doi.org/10.1016/j.ejmg.2014.02.006 - Duplication of EYA1 causes Branchiootic Syndrome in a Brazilian family
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Informações sobre o DOI: 10.1016/j.ejmg.2014.02.006 (Fonte: oaDOI API)
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