Role of ARHGAP29 nucleotide variants in the etiology of non-syndromic cleft lip with or without cleft palate.

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....

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Bibliographic Details
Main Authors: Justyna Dąbrowska, Barbara Biedziak, Agnieszka Lasota, Paweł P. Jagodziński, Adrianna Mostowska
Format: Article
Language:English
Published: Poznan University of Medical Sciences 2020-06-01
Series:Journal of Medical Science
Subjects:
nsCL/P
ARHGAP2
SNVs
Online Access:https://jms.ump.edu.pl/index.php/JMS/article/view/414

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