A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes.

Gershoni, Moran

A familial study of azoospermic men identifies three novel causative mutations in three new human azoospermia genes. [electronic resource] - Genetics in medicine : official journal of the American College of Medical Genetics 09 2017 - 998-1006 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1530-0366

10.1038/gim.2016.225 doi


Amino Acid Sequence
Azoospermia--diagnosis
Biomarkers
Biopsy
Case-Control Studies
Consanguinity
DNA Mutational Analysis
DNA-Binding Proteins--genetics
Dyneins--genetics
Family
Genetic Association Studies
Genetic Predisposition to Disease
Genetic Testing
Genotype
Humans
In Situ Hybridization, Fluorescence
Male
Mutation
Pedigree
Spermatozoa--metabolism