P. Rathnayake

What We Fail to See in Neuro-Genetic Diseases: A Bird’s Eye View from the Developing World

A. Dalal, K. Satyamoorthy, A. Anand, 2020, Annals of neurosciences.

A novel variant in the COL6A1 gene causing Ullrich congenital muscular dystrophy in a consanguineous family: a case report

V. Dissanayake, C. Bönnemann, S. Donkervoort, 2021, BMC Neurology.

Evaluation of an in house genetic testing method for confirmation of Prader - Willi and Angelman syndromes in Sri Lanka

N. Chandrasekharan, P. Rathnayake, N. Atapattu, 2021 .