Associated Papers
C1-linker region of PARG1 RhoGAP promotes the catalytic recognition fold of RhoA substrate.
Kouchi Z et al.
Plos One, 2025
A novel splicing mutation of ARHGAP29 is associated with nonsyndromic cleft lip with or without cleft palate.
Yu Q et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2022
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies.
Santos-Cortez RLP et al.
Genes, 2021
33924653 (PubMed )
Supplement: genes-12-00566-s001.pdf
Expression and mutation analyses implicate ARHGAP29 as the etiologic gene for the cleft lip with or without cleft palate locus identified by genome-wide association on chromosome 1p22.
Leslie EJ et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2012
Select a paper to view details