Associated Papers
Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency.
Boisson B et al.
Journal of Clinical Immunology, 2017
Mutations in WNT10A are frequently involved in oligodontia associated with minor signs of ectodermal dysplasia.
Plaisancié J et al.
American Journal of Medical Genetics. Part A, 2013
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