CARMIL2 variant linked to infantile onset of colitis and gastrointestinal eosinophilic disease July 4, 2019 No Comments
CNOT2 deletion identified as responsible for the phenotypes of the 12q15 microdeletion syndrome July 2, 2019 No Comments
Researchers link LIG3 mutations to mitochondrial neurogastrointestinal encephalomyopathy June 28, 2019 No Comments
Mutations in SSBP1 gene cause a form of optic atrophy with mitochondrial depletion June 28, 2019 No Comments
Researchers unveil LRP6 gene to be associated with familial hypercholesterolemia June 26, 2019 No Comments
DGM1 as a novel biomarker of response to enzastaurin in DLBCL and glioblastoma June 25, 2019 No Comments
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