A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family-Reference-Cited by-同舟云学术

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A novel mutation in the GAN gene causes an intermediate form of giant axonal neuropathy in an Arab–Israeli family

Published:2013-05 Issue:3 Volume:17 Page:259-264
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Abu-Rashid M.,Mahajnah M.,Jaber L.,Kornreich L.,Bar-On E.,Basel-Vanagaite L.,Soffer D.,Koenig M.,Straussberg R.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference18 articles.

1. Giant axonal neuropathy;Berg;Pediatrics.,1972

2. Childhood giant axonal neuropathy. Case report and review of the literature;Tandan;J Neurol Sci,1987

3. Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1;Ben Hamida;Neurogenetics,1997

4. The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy;Bomont;Nat Genet,2000

5. Giant axonal neuropathy;Yang;Cell Mol Life Sci,2007

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