Mutations in CRLF1 cause familial achalasia. [electronic resource]
Producer: 20180316Description: 104-108 p. digitalISSN:- 1399-0004
- Abnormalities, Multiple -- genetics
- Death, Sudden
- Esophageal Achalasia -- genetics
- Facies
- Genetic Predisposition to Disease
- Hand Deformities, Congenital -- genetics
- High-Throughput Nucleotide Sequencing
- Homozygote
- Humans
- Hyperhidrosis -- genetics
- Mutation
- Pedigree
- Receptors, Cytokine -- genetics
- Trismus -- congenital
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.