SPG11mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration-Reference-Cited by-同舟云学术

SPG11mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration

Published:2009-10-05 Issue:7 Volume:150B Page:984-992
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Örlén Hanna,Melberg Atle,Raininko Raili,Kumlien Eva,Entesarian Miriam,Söderberg Per,Påhlman Magnus,Darin Niklas,Kyllerman Mårten,Holmberg Eva,Engler Henry,Eriksson Urban,Dahl Niklas

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference42 articles.

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2. Spastic paraplegia 15: Linkage and clinical description of three Tunisian families;Boukhris;Mov Disord,2008

3. Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity;Boukhris;Arch Neurol,2008

4. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum;Casali;Neurology,2004

5. SP G11: A consistent clinical phenotype in a family with homozygous Spatacsin truncating mutation;Del Bo;Neurogenetics,2007

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