Murali D. Bashyam

Splice, Insertion‐Deletion and Nonsense Mutations that Perturb the Phenylalanine Hydroxylase Transcript Cause Phenylketonuria in India

M. Kabra, M. Bashyam, A. Dalal, 2014, Journal of cellular biochemistry.

Molecular genetic analysis of MSUD from India reveals mutations causing altered protein truncation affecting the C‐termini of E1α and E1β

A. Dalal, H. Nagarajaram, A. Chaudhary, 2012, Journal of cellular biochemistry.

A novel EDARADD 5′‐splice site mutation resulting in activation of two alternate cryptic 5′‐splice sites causes autosomal recessive Hypohidrotic Ectodermal Dysplasia

M. Bashyam, K. Girisha, A. Chaudhary, 2016, American journal of medical genetics. Part A.