Items where Author is "Haghighatzadeh, M."
 | Up a level |
Group by: Item Type | No Grouping
Number of items: 2.
(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
(2025) Approach to Oculomotor Apraxia: A Syndromic Approach to Genetic Causes. Cerebellum. p. 14. ISSN 1473-4222