Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69.

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Title: Three Iranian patients with rare subtypes of hereditary spastic paraplegia (HSP): SPG76, SPG56, and SPG69.
Authors: Sadr Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Ghasemi A; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran., Rohani M; Department of Neurology, The Five Senses Health Institute, Iran University of Medical Sciences, Tehran, Iran., Khorram Khorshid HR; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Habibi-Kavashkohie MR; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; CHU Sainte Justine Research Center, University of Montreal, Montréal, Canada., Mohammadi Y; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Alavi A; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran. afaghalavi@gmail.com.; Neuromuscular Research Center, Tehran University of Medical Sciences, Tehran, Iran. afaghalavi@gmail.com.
Source: Neurogenetics [Neurogenetics] 2024 Nov 28; Vol. 26 (1), pp. 12. Date of Electronic Publication: 2024 Nov 28.
Publication Type: Journal Article
Journal Info: Publisher: Springer-Verlag Country of Publication: United States NLM ID: 9709714 Publication Model: Electronic Cited Medium: Internet ISSN: 1364-6753 (Electronic) Linking ISSN: 13646745 NLM ISO Abbreviation: Neurogenetics Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1364-6753
DOI:10.1007/s10048-024-00789-1