Keywords = dystroglycanopathies
Number of Articles: 1

A child of congenital muscular dystrophy-dystroglycanopathy with homozygous missense variation in exon 3 of the ISPD Gene: A rare case from Odisha

Volume 2020, November, November 2020, Pages 1-3

Sebaranjan Biswal, Debasish Panigrahi, Nirmal Kumar Mohakud, Manoj Kumar, Natabara Swain

Advanced Biomedical Research