Savasta, Salvatore <br/><br/>
X-Linked Hypohidrotic Ectodermal Dysplasia: New Features and a Novel EDA Gene Mutation.  [electronic resource] 

 -  Cytogenetic and genome research  2017 
 - 111-116 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1424-859X 
<br/><br/><label>Standard No.: </label>10.1159/000478922  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Anodontia--genetics<br/>Child, Preschool<br/>Codon<br/>DNA Mutational Analysis<br/>Ectodermal Dysplasia 1, Anhidrotic--genetics<br/>Ectodysplasins--genetics<br/>Female<br/>Genes, X-Linked<br/>Hemizygote<br/>Heterozygote<br/>Histidine--genetics<br/>Humans<br/>Hypohidrosis--genetics<br/>Leucine--genetics<br/>Lip--abnormalities<br/>Male<br/>Maxilla--abnormalities<br/>Mutation, Missense<br/>Nasal Bone--abnormalities