Items where Author is "Neshatdoust, M."
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Number of items: 2.
Article
(2025) Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders. Genetics in medicine : official journal of the American College of Medical Genetics. p. 101251. ISSN 1530-0366 (Electronic) 1098-3600 (Linking)
(2023) Childhood-Onset Choreo-Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review. Movement Disorders Clinical Practice. pp. 101-108. ISSN 2330-1619 (Electronic) 2330-1619 (Linking)