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Indian Pediatrics|June 26, 2012
Diagnostic strategy for mucolipidosis II/IIIJ Sheth, M Mistri, M Kamate, et al.
Journal of Pediatric Genetics|August 11, 2017
Genetic Screening of Selected Disease-Causing Mutations in Glutaryl-CoA Dehydrogenase Gene among Indian Patients with Glutaric Aciduria Type IKruthika-Vinod Tp, Shaik Muntaj, K S Devaraju, et al.
Clinical Genetics|May 7, 2016
Whole gene duplication of SCN2A and SCN3A is associated with neonatal seizures and a normal intellectual developmentA-C Thuresson, G Van Buggenhout, F Sheth, et al.
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