Khan, S <br/><br/>
A homozygous missense mutation in SLC25A16 associated with autosomal recessive isolated fingernail dysplasia in a Pakistani family.  [electronic resource] 

 -  The British journal of dermatology  02 2018 
 - 556-558 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1365-2133 
<br/><br/><label>Standard No.: </label>10.1111/bjd.15661  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Autoantigens--genetics<br/>Female<br/>Genes, Recessive--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Mutation, Missense--genetics<br/>Nails, Malformed--genetics<br/>Pakistan<br/>Pedigree<br/>Young Adult