Novel mutation in TTC21A triggers partial nonsense-mediated mRNA decay and causes male infertility with MMAF.

Liu, Gang; Yin, Xinyu; Xing, Xiaowei; Yin, Silu; Shen, Yuehan; Zhang, Huan; Lin, Ge; Lu, Guangxiu; Li, Weina

Liu, Gang; Yin, Xinyu; Xing, Xiaowei; Yin, Silu; Shen, Yuehan; Zhang, Huan; Lin, Ge; Lu, Guangxiu; Li, Weina.

Afiliación

Liu G; The Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha, China.
Yin X; The Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha, China.
Xing X; Center for Medical Experiments, The Third Xiangya Hospital, Central South University, Changsha, China.
Yin S; Department of Andrology, Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, China.
Shen Y; The Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha, China.
Zhang H; The Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha, China.
Lin G; Department of Andrology, Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, China.
Lu G; The Institute of Reproduction and Stem Cell Engineering, School of Basic Medical Sciences, Central South University, Changsha, China.
Li W; Department of Andrology, Reproductive and Genetic Hospital of CITIC-Xiangya, Changsha, China.

Clin Genet ; 102(5): 459-460, 2022 11.

Article en En | MEDLINE | ID: mdl-35920310

Asunto(s)

Infertilidad Masculina; Degradación de ARNm Mediada por Codón sin Sentido; Humanos; Infertilidad Masculina/genética; Masculino; Mutación; Degradación de ARNm Mediada por Codón sin Sentido/genética; Cola del Espermatozoide

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Degradación de ARNm Mediada por Codón sin Sentido / Infertilidad Masculina Tipo de estudio: Etiology_studies Límite: Humans / Male Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo

Imprimir

XML

PubMed Links

Buscar en Google