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Novel MEI1 compound heterozygous mutation in a sporadic family associated with spermatogenetic failure

Detalles Bibliográficos
Autores principales:	Chen, Jie, Li, Feng-Hua, Xing, Jin-Hao, Zhang, Xue-Bao, Du, Zhao-Li, Jin, Yin-Shan, Cui, Yuan-Qing, Wang, Xiong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10411250/ https://www.ncbi.nlm.nih.gov/pubmed/36348580 http://dx.doi.org/10.4103/aja202280

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