Busch, A <br/><br/>
Mutations in CRLF1 cause familial achalasia.  [electronic resource] 

 -  Clinical genetics  Jul 2017 
 - 104-108 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.12953  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Death, Sudden<br/>Esophageal Achalasia--genetics<br/>Facies<br/>Genetic Predisposition to Disease<br/>Hand Deformities, Congenital--genetics<br/>High-Throughput Nucleotide Sequencing<br/>Homozygote<br/>Humans<br/>Hyperhidrosis--genetics<br/>Mutation<br/>Pedigree<br/>Receptors, Cytokine--genetics<br/>Trismus--congenital