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 th...
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| Hauptverfasser: | , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Royan Institute (ACECR), Tehran
2016-07-01
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| Schriftenreihe: | International Journal of Fertility and Sterility |
| Schlagworte: | |
| Online-Zugang: | http://www.ijfs.ir/article_45379_a5d91bb69cce4abae1f6693bdb680186.pdf |
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