De novo ALX4 variant detected in child with non-syndromic craniosynostosis

Current understanding of the genetic factors contributing to the etiology of non-syndromic craniosynostosis (NSC) remains scarce. The present work investigated the presence of variants in ALX4, EFNA4, and TWIST1 genes in children with NSC to verify if variants within these genes may contribute to th...

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Bibliographic Details
Main Author: Fonteles,C.S. (author)
Other Authors: Finnell,R.H. (author), Lei,Y. (author), Zurita-Jimenez,M.E. (author), Monteiro,A.J. (author), George,T.M. (author), Harshbarger,R.J. (author)
Format: article
Language:eng
Published: 2021
Subjects:
Congenital abnormalities
Mutation
Missense mutation
DNA
Saliva
Cranial sutures
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2021001100616
Country:Brazil
Oai:oai:scielo:S0100-879X2021001100616

Internet

http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2021001100616

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