P. Kondurkar

Clinical Characteristics, Molecular Profile, and Outcomes in Indian Patients with Glutaric Aciduria Type 1

K. Girisha, R. Christopher, S. Naushad, 2020, Journal of Pediatric Genetics.

Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India

S. Idicula-Thomas, F. Sheth, J. Sheth, 2012, PloS one.

Clinical, biochemical and mutation profile in Indian patients with Sandhoff disease

J. Sheth, M. Mistri, P. Tamhankar, 2015, Journal of Human Genetics.

Identification of novel mutations in HEXA gene in children affected with Tay-Sachs disease from India

S. Idicula-Thomas, F. Sheth, J. Sheth, 2014, Molecular Cytogenetics.

Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India

F. Sheth, J. Sheth, Sarita Gupta, 2012, Molecular Cytogenetics.

Krabbe disease--clinical profile.

M. Tullu, M. Muranjan, B. Bharucha, 2000, Indian pediatrics.

Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India

F. Sheth, J. Sheth, Sarita Gupta, 2012, PloS one.