Autosomal dominant, familial spastic paraplegia, type I: Clinical and genetic analysis of a large North American family-Reference-Cited by-同舟云学术

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Autosomal dominant, familial spastic paraplegia, type I: Clinical and genetic analysis of a large North American family

Published:1995-02-01 Issue:2 Volume:45 Page:325-331
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Fink J. K.,Sharp G. B.,Lange B. M.,Wu C-t. B.,Haley T.,Otterud B.,Peacock M.,Leppert M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 38 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ataxia and spasticity;Neurogenetics for the Practitioner;2024

2. Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature;Movement Disorders Clinical Practice;2023-03-16

3. The hereditary spastic paraplegias;Handbook of Clinical Neurology;2023

4. Autosomal dominant spastic paraplegias;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2021

5. The hereditary spastic paraplegias;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020

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