Role of ARHGAP29 nucleotide variants in the etiology of non-syndromic cleft lip with or without cleft palate.
Aim. Non-syndromic cleft lip with or without cleft palate (nsCL/P) is a common birth defect of complex and heterogeneous aetiology. Genome-wide association studies (GWAS) of nsCL/P have identified an association for the 1p22.1 chromosomal region, in which ARHGAP29 was suggested as a candidate gene....
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Poznan University of Medical Sciences
2020-06-01
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Series: | Journal of Medical Science |
Subjects: | |
Online Access: | https://jms.ump.edu.pl/index.php/JMS/article/view/414 |