Items where Author is "Hamid, M."

(2026) Bi-allelic TPP1 variants in neuronal ceroid lipofuscinosis 2: clinical findings from an Iranian cohort of 20 patients, founder effect, and in silico analyses. Human Genetics. p. 19. ISSN 0340-6717

(2019) Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran. Immunology Letters. pp. 70-78. ISSN 0165-2478

(2019) Niemann-Pick Diseases: The Largest Iranian Cohort with Genetic Analysis. Iranian Journal of Child Neurology. pp. 155-162. ISSN 1735-4668

(2015) Incidence and clinical importance of BCR-ABL1 mutations in Iranian patients with chronic myeloid leukemia on imatinib. Journal of Human Genetics. pp. 253-258. ISSN 14345161 (ISSN)