Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype

Title
Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype
Authors
Keywords
-
Journal
CLINICAL GENETICS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2019-10-26
DOI
10.1111/cge.13662

Ask authors/readers for more resources

Find the ideal target journal for your manuscript

Explore over 38,000 international journals covering a vast array of academic fields.

Search

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started