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SLC25A19mutation as a cause of neuropathy and bilateral striatal necrosis

  • Published:2009-09 Issue:3 Volume:66 Page:419-424
  • ISSN:0364-5134
  • Container-title:Annals of Neurology
  • language:en
  • Short-container-title:Ann Neurol.

Author:

Spiegel Ronen,Shaag Avraham,Edvardson Simon,Mandel Hanna,Stepensky Polina,Shalev Stavit A.,Horovitz Yoseph,Pines Ophry,Elpeleg Orly

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference17 articles.

1. Acute neurological dysfunction associated with destructive lesions of the basal ganglia in children;Goutieres;Ann Neurol,1982

2. Acute infantile bilateral striatal necrosis: single-photon emission computed tomography (SPECT) imaging and review;Zevit;J Child Neurol,2007

3. Heteroplasmic mtDNA mutation (T-to-G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high;Tatuch;Am J Hum Genet,1992

4. Type I glutaric aciduria, part 2: a model of acute striatal necrosis;Strauss;Am J Med Genet C Semin Med Genet,2003

5. White matter changes in Wilson disease;Hedera;Arch Neurol,2002

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