Mutations in EDA and EDAR Genes in a Large Mexican Hispanic Cohort with Hypohidrotic Ectodermal Dysplasia

Ítems similars

• Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients
  per: Zeng, Binghui, et al.
  Publicat: (2016)
• Novel EDA or EDAR Mutations Identified in Patients with X-Linked Hypohidrotic Ectodermal Dysplasia or Non-Syndromic Tooth Agenesis
  per: Zeng, Binghui, et al.
  Publicat: (2017)
• Hypohidrotic Ectodermal Dysplasia and Immunodeficiency with Coincident NEMO and EDA Mutations
  per: Keller, Michael D., et al.
  Publicat: (2011)
• EDAR mutation in autosomal dominant hypohidrotic ectodermal dysplasia in two Swedish families
  per: Lind, Lisbet K, et al.
  Publicat: (2006)
• High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus
  per: Zonana, J., et al.
  Publicat: (1992)