Hypohidrotic Ectodermal Dysplasia
Last Posted: Apr 26, 2018
- Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia.
Schneider Holm et al. The New England journal of medicine 2018 Apr (17) 1604-1610
- Protein therapy in the womb overrides genetic glitch hampering teeth development, ability to sweat
R Lewis, Genetic Literacy Project, Apr 25, 2018
- Eight Mutations of Three Genes (EDA, EDAR, and WNT10A) Identified in Seven Hypohidrotic Ectodermal Dysplasia Patients.
Zeng Binghui, et al. Genes 2016 0 (9)
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements.
Wohlfart Sigrun, et al. Journal of human genetics 2016 6
- Mutations in EDA and EDAR Genes in a Large Mexican Hispanic Cohort with Hypohidrotic Ectodermal Dysplasia.
Salas-Alanis Julio C, et al. Annals of dermatology 2015 8 (4) 474-7
- Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population.
He Huiying, et al. PloS one 2013 0 (11) e80393
- Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
Plaisancié Julie, et al. American journal of medical genetics. Part A 2013 4 (4) 671-8
- Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.
Bergendal Birgitta, et al. American journal of medical genetics. Part A 2011 7 (7) 1616-22
- Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia.
Schneider Holm, et al. Journal of medical genetics 2011 6 (6) 426-32
- Hypohidrotic ectodermal dysplasia
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