Whole Genome Sequencing Reveals Novel Non-Synonymous Mutation in Ectodysplasin A (EDA) Associated with Non-Syndromic X-Linked Dominant Congenital Tooth Agenesis
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
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2. An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis;Molecular Genetics and Genomics;2022-11-14
3. Identified a novel splicing mutation at EDA gene in a hypohidrotic ectodermal dysplasia pedigree;Oral Diseases;2022-09-09
4. The First Report of a Missense Variant in RFX2 Causing Non-Syndromic Tooth Agenesis in a Consanguineous Pakistani Family;Frontiers in Genetics;2022-01-25
5. An in vitro and computational validation of a novel loss-of-functional mutation in PAX9 associated with non-syndromic tooth agenesis;2022-01-01
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