Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice
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DOI: 10.1136/jmedgenet-2021-108137
Abstract: Background Asthenozoospermia is a major factor contributing to male infertility. The mitochondrial sheath (MS), an important organelle in the midpiece of spermatozoa, is crucial to sperm motility. ARMC12 is a mitochondrial peripheral membrane protein. Deletion… read more here.
Keywords: multiple midpiece; midpiece defects; microscopy; asthenozoospermia ... See more keywords