A new locus (SPG47) maps to 1p13.2–1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum-Reference-Cited by-同舟云学术

A new locus (SPG47) maps to 1p13.2–1p12 in an Arabic family with complicated autosomal recessive hereditary spastic paraplegia and thin corpus callosum

Published:2011-06 Issue:1-2 Volume:305 Page:67-70
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Blumkin Lubov,Lerman-Sagie Tally,Lev Dorit,Yosovich Keren,Leshinsky-Silver Esther

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference18 articles.

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2. Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosum;Crimella;J Med Genet,2009

3. A new locus (SPG46) maps to 9p21.2–q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum;Boukhris;Neurogenetics,2010

4. Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms;Salinas;Lancet Neurol,2008

5. Inborn errors of metabolism: A cause of abnormal brain development;Nissenkorn;Neurology,2001

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