PMPCAmutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia-Reference-Cited by-同舟云学术

PMPCAmutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia

Published:2015-03-25 Issue:6 Volume:138 Page:1505-1517
ISSN:0006-8950
Container-title:Brain
language:en
Short-container-title:Brain

Author:

Jobling Rebekah K.,Assoum Mirna,Gakh Oleksandr,Blaser Susan,Raiman Julian A.,Mignot Cyril,Roze Emmanuel,Dürr Alexandra,Brice Alexis,Lévy Nicolas,Prasad Chitra,Paton Tara,Paterson Andrew D.,Roslin Nicole M.,Marshall Christian R.,Desvignes Jean-Pierre,Roëckel-Trevisiol Nathalie,Scherer Stephen W.,Rouleau Guy A.,Mégarbané André,Isaya Grazia,Delague Valérie,Yoon Grace

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Reference30 articles.

1. Diagnostic Approach to Childhood-Onset Cerebellar Atrophy

2. Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse

3. Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification

4. Human Frataxin Activates Fe–S Cluster Biosynthesis by Facilitating Sulfur Transfer Chemistry

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