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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Detalhes bibliográficos
Autor principal: Fonteles,C.S. (author)
Outros Autores: Finnell,R.H. (author), Lei,Y. (author), Zurita-Jimenez,M.E. (author), Monteiro,A.J. (author), George,T.M. (author), Harshbarger,R.J. (author)
Formato: article
Idioma:eng
Publicado em: 2021
Assuntos:
Congenital abnormalities
Mutation
Missense mutation
DNA
Saliva
Cranial sutures
Texto completo:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2021001100616
País:Brasil
Oai:oai:scielo:S0100-879X2021001100616

Texto Completo

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

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