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

Apr 2, 2021 |

Journal:

JOURNAL OF MEDICAL GENETICS
Document Code:

SY132781
Volume:

56
Issue:

2
Page Number:

96-103
Translation or Not:

no
Date of Publication:

Jan 1, 2019

Pre One: The rare mutation in the endosome-associated recycling protein gene VPS50 is associated with human neural tube defects
Next One: Author Correction: CRISPR–Cas9-mediated base-editing screening in mice identifies DND1 amino acids that are critical for primordial germ cell development (Nature Cell Biology, (2018), 20, 11, (1315-1325), 10.1038/s41556-018-0202-4)