TY  - GEN
AU  - Busch,A
AU  - Žarković,M
AU  - Lowe,C
AU  - Jankofsky,M
AU  - Ganschow,R
AU  - Buers,I
AU  - Kurth,I
AU  - Reutter,H
AU  - Rutsch,F
AU  - Hübner,C A
TI  - Mutations in CRLF1 cause familial achalasia
SN  - 1399-0004
PY  - 2018///0316
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Death, Sudden
KW  - Esophageal Achalasia
KW  - Facies
KW  - Genetic Predisposition to Disease
KW  - Hand Deformities, Congenital
KW  - High-Throughput Nucleotide Sequencing
KW  - Homozygote
KW  - Humans
KW  - Hyperhidrosis
KW  - Mutation
KW  - Pedigree
KW  - Receptors, Cytokine
KW  - Trismus
KW  - congenital
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1111/cge.12953
ER  -