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

Internet

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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