Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family (2012)
- Authors:
- USP affiliated authors: AURICCHIO, MARIA TERESA BALESTER DE MELLO - IB ; NETTO, REGINA CELIA MINGRONI - IB
- Unidade: IB
- DOI: 10.1016/j.gene.2012.09.023
- Subjects: PERDA AUDITIVA; LINHAGEM CELULAR
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
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ABNT
LEZIROVITZ, Karina et al. Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family. Gene, v. 511, n. 2, p. 280-284, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.gene.2012.09.023. Acesso em: 28 dez. 2025. -
APA
Lezirovitz, K., Batissoco, A. C., Lima, F. T., Auricchio, M. T. B. de M., Nonose, R. W., Santos, S. R., et al. (2012). Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family. Gene, 511( 2), 280-284. doi:10.1016/j.gene.2012.09.023 -
NLM
Lezirovitz K, Batissoco AC, Lima FT, Auricchio MTB de M, Nonose RW, Santos SR, Guilherme L, Oiticica J, Mingroni Netto RC. Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family [Internet]. Gene. 2012 ; 511( 2): 280-284.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1016/j.gene.2012.09.023 -
Vancouver
Lezirovitz K, Batissoco AC, Lima FT, Auricchio MTB de M, Nonose RW, Santos SR, Guilherme L, Oiticica J, Mingroni Netto RC. Aberrant transcript produced by a splice donor site deletion in the TECTA gene is associated with autosomal dominat deafness in a Brazilian family [Internet]. Gene. 2012 ; 511( 2): 280-284.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1016/j.gene.2012.09.023 - Genomic ancestry of rural african-derived populations from southeastern Brazil
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Informações sobre o DOI: 10.1016/j.gene.2012.09.023 (Fonte: oaDOI API)
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