A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan-Reference-Cited by-同舟云学术

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A distinct autosomal recessive ataxia maps to chromosome 12in an inbred family from Jordan

Published:2006-07 Issue:6 Volume:28 Page:353-357
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

El-Shanti Hatem,Daoud Azhar,Sadoon Ammar A.,Leal Suzanne M.,Chen Shan,Lee Kwanghyuk,Spiegel Ronald

Publisher

Elsevier BV

Subject

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

Reference18 articles.

1. The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias;Di Donato;Neurol Sci,2001

2. Progressive myoclonus epilepsies: specific causes and diagnosis;Berkovic;N Engl J Med,1986

3. Die progressive myoclonus-epilepsie (Unverricht's myoclonie);Lundborg,1903

4. Die myoclonie;Unverricht,1891

5. Molecular background of progressive myoclonus epilepsy;Lehesjoki;EMBO J,2003

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4. Progressive myoclonus epilepsy;Handbook of Clinical Neurology;2013

5. PRICKLE1 progressive myoclonus epilepsy in Southern Italy;Movement Disorders;2010-09-14

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