Further Clinical and Genetic Characterization of SPG11: Hereditary Spastic Paraplegia with Thin Corpus Callosum-Reference-Cited by-同舟云学术

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Further Clinical and Genetic Characterization of SPG11: Hereditary Spastic Paraplegia with Thin Corpus Callosum

Published:2006-04 Issue:2 Volume:37 Page:59-66
ISSN:0174-304X
Container-title:Neuropediatrics
language:en
Short-container-title:Neuropediatrics

Author:

Ölmez A.,Uyanik G.,Özgül R.,Gross C.,Cirak S.,Elibol B.,Anlar B.,Winner B.,Hehr U.,Topaloglu H.,Winkler J.

Publisher

Georg Thieme Verlag KG

Subject

Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2006-923982.pdf

Cited by 20 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. Genotype–phenotype correlation in seven motor neuron disease families with novel ALS2 mutations;American Journal of Medical Genetics Part A;2020-11-05

2. A case of spastic paraplegia type 11 with a variation in the SPG11 gene;Egyptian Journal of Medical Human Genetics;2020-07-15

3. Autophagy in Myelinating Glia;The Journal of Neuroscience;2019-11-19

4. Whole-genome sequencing of two probands with hereditary spastic paraplegia reveals novel splice-donor region variant and known pathogenic variant in SPG11;Molecular Case Studies;2016-09-07

5. Novel Compound Heterozygous Spatacsin Mutations in a Greek Kindred with Hereditary Spastic Paraplegia SPG11 and Dementia;Neurodegenerative Diseases;2016

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