Karen Jain

A T → C mutation at nt 8993 of mitochondrial DNA in a child with Leigh syndrome

Filippo M. Santorelli, Sara Shanske, Karen Jain et al. · Neurology · 1994 · 89 citations

Prevalence of medium-chain acyl-coenzyme A dehydrogenase deficiency in the sudden infant death syndrome

Raanan Arens, David Gozal, Karen Jain et al. · The Journal of Pediatrics · 1993 · 60 citations

Inherited Metabolic Disease, Pediatrics, Pathology +4

Clinical Heterogeneity Associated with the Mitochondrial DNA T8993C Point Mutation

Filippo M. Santorelli, Suk-Chun Mak, Marta Elisa Vázquez-Memije et al. · Pediatric Research · 1996 · 60 citations · Full text

Clinical Heterogeneity Associated, Mitochondrial Function, Genetic Disorder +8

Diagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes in a Chinese family by PCR/restriction enzyme analysis

C W Lam, Karen Jain, K Y Chan et al. · Molecular Pathology · 1995 · 10 citations · Full text

MERRF syndrome with overwhelming lactic acidosis

Terence D. Sanger, Karen Jain · Pediatric Neurology · 1996 · 10 citations

Gastroenterology, Pathology, Merrf Syndrome +3