VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis-Reference-Cited by-同舟云学术

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VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis

Published:2019-08-16 Issue:4 Volume:20 Page:187-195
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Hausman-Kedem Moran^ORCID,Ben-Shachar Shay,Menascu Shay,Geva Karen,Sagie Liora,Fattal-Valevski Aviva

Funder

Bircher-Bener Grant for Preventative Medicine from Sackler Faculty of Medicine, Tel Aviv University

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-019-00586-1.pdf

Reference41 articles.

1. McMonagle P, Webb S, Hutchinson M (2002) The prevalence of “pure” autosomal dominant hereditary spastic paraparesis in the island of Ireland. J Neurol Neurosurg Psychiatry 72(1):43–46

2. Sedel F, Fontaine B, Saudubray JM, Lyon-Caen O (2007) Hereditary spastic paraparesis in adults associated with inborn errors of metabolism: a diagnostic approach. J Inherit Metab Dis 30(6):855–864

3. Harding AE (1981) Hereditary “pure” spastic paraplegia: a clinical and genetic study of 22 families. J Neurol Neurosurg Psychiatry 44:871–883

4. McDermott CJ, White K, Bushby K, Shaw PJ (2000) Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry 69:150–160

5. Depienne C, Stevanin G, Brice A, Durr A (2007) Hereditary spastic paraplegias: an update. Curr Opin Neurol 20:674–680

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