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Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple...

Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2132251091

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

About this item

Full title

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

Publisher

England: BMJ Publishing Group LTD

Journal title

Journal of medical genetics, 2019-02, Vol.56 (2), p.96-103

Language

English

Formats

Publication information

Publisher

England: BMJ Publishing Group LTD

More information

Scope and Contents

Contents

BackgroundMale infertility is a major issue of human reproduction health. Asthenoteratospermia can impair sperm motility and cause male infertility. Asthenoteratospermia with multiple morphological abnormalities of the flagella (MMAF) presents abnormal spermatozoa with absent, bent, coiled, short and/or irregular-calibre flagella. Previous studies...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2132251091

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2132251091

Other Identifiers

ISSN

0022-2593

E-ISSN

1468-6244

DOI

10.1136/jmedgenet-2018-105486

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