Whole-exome sequencing identifies two novel ALMS1 mutations in Indian patients with Leber congenital amaurosis March 29, 2021
The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India March 25, 2021
Clinical Study of 668 Indian Subjects with Juvenile, Young, and Early Onset Parkinson’s Disease March 9, 2021
The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India March 5, 2021
Novel CTSF Indel in a patient with Kufs disease and resistant schizophrenia: A case report February 9, 2021
BCR-ABL1 kinase domain mutation analysis by next generation sequencing detected additional mutations in chronic myeloid leukemia patients with suboptimal response to imatinib January 22, 2021
