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Article

A newly discovered mutation in PICK1 in a human with globozoospermia

21 Jun 2010

Abstract excerpt

Globozoospermia is a human infertility syndrome caused by spermatogenesis defects (OMIM 102530). Acrosome plays an important role at the site of sperm-zonapellucida binding during the fertilization process. Thus, malformation of the acrosome is the most prominent feature seen in globozoospermia. Disruption of several mouse genes, including Gopc (Golgi-associated PDZ and coiled-coil motif containing protein), Hrb...

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Share to Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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Identifiers

PMID: 20562896
DOI: 10.1038/aja.2010.47

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A newly discovered mutation in PICK1 in a human with globozoospermiaPMID 20562896Read ↗

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