November 10, 2018Journal of Medical Genetics

Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella

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Abstract

Our experimental findings elucidate that homozygous loss-of-function mutations in CFAP69 can lead to asthenoteratospermia with MMAF in humans and mice.

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Cite This Study

He et al. (2018) studied this question.

synapsesocial.com/papers/69d88d67c025a7c015bee05e https://doi.org/10.1136/jmedgenet-2018-105486

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Abstract

Our experimental findings elucidate that homozygous loss-of-function mutations in CFAP69 can lead to asthenoteratospermia with MMAF in humans and mice.