CARMIL2 variant linked to infantile onset of colitis and gastrointestinal eosinophilic disease July 4, 2019
CNOT2 deletion identified as responsible for the phenotypes of the 12q15 microdeletion syndrome July 2, 2019
Researchers link LIG3 mutations to mitochondrial neurogastrointestinal encephalomyopathy June 28, 2019
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