SANMATI CUDDAPAH to Mutation
This is a "connection" page, showing publications SANMATI CUDDAPAH has written about Mutation.
Connection Strength
0.082
-
Bi-allelic variants in OGDHL cause a neurodevelopmental spectrum disease featuring epilepsy, hearing loss, visual impairment, and ataxia. Am J Hum Genet. 2021 12 02; 108(12):2368-2384.
Score: 0.068
-
Fetal cardiomyopathy in neurofibromatosis type I: Novel phenotype and review of the literature. Am J Med Genet A. 2019 06; 179(6):1042-1046.
Score: 0.014