Items where Author is "Anwar, I."
 | Up a level |
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 2.
Article
(2025) ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy. Genetics in Medicine. p. 15. ISSN 1098-3600
(2024) ELFN1 deficiency is associated with an autosomal recessive neurodevelopmental disorder with epilepsy. European Journal of Human Genetics. pp. 1510-1511. ISSN 1018-4813