Biallelic start loss variant, c. <scp>1A</scp> > G in <scp> <i>GCSH</i> </scp> is associated with variant nonketotic hyperglycinemiaPurvi Majethia, Anju Shukla, Puneeth H. Somashekar et al.|Clinical Genetics|2021Cited by 9
Genetic and phenotypic landscape of pediatric‐onset epilepsy in 142 Indian families: Counseling and therapeutic implicationsPurvi Majethia, Anju Shukla, Leslie Lewis et al.|Clinical Genetics|2024Cited by 7
Author response for "Biallelic Start Loss Variant, c. 1A >G in GCSH is Associated with Variant Nonketotic Hyperglycinemia"Purvi Majethia, Anju Shukla, Malavika Hebbar et al.|Unknown|2021Cited by 0
Author response for "Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications"Purvi Majethia, Anju Shukla, Leslie Lewis et al.|Unknown|2024Cited by 0