Assessment of DPY19L2 Deletion in Familial and Non-Familial Individuals with Globozoospermia and DPY19L2 Genotyping

BACKGROUND: Globozoospermia is a rare syndrome with an incidence of less than 0.1% among infertile men. Researchers have recently identified a large deletion, about 200 kbp, encompassing the whole length of DPY19L2 or mutations in SPATA16 and PICK1 genes associated with globozoospermia. The aim of t...

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Detalles Bibliográficos
Autores principales: Modarres, Parastoo, Tanhaei, Somayeh, Tavalaee, Marziyeh, Ghaedi, Kamran, Deemeh, Mohammad Reza, Nasr-Esfahani, Mohammad Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royan Institute 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948072/
https://www.ncbi.nlm.nih.gov/pubmed/27441053

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