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