Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability. [electronic resource]
- American journal of human genetics Apr 2015
- 581-96 p. digital
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
1537-6605
10.1016/j.ajhg.2015.02.014 doi
Animals Base Sequence Epistasis, Genetic--genetics Genetic Predisposition to Disease--genetics Genetic Variation Genome-Wide Association Study Hirschsprung Disease--genetics Mice Molecular Sequence Data Proto-Oncogene Proteins c-ret--genetics Semaphorins--deficiency Sequence Analysis, DNA