Spinocerebellar Ataxia 21 with Retardation

J Gordon Millichap; John J Millichap

doi:10.15844/pedneurbriefs-28-11-1

Spinocerebellar Ataxia 21 with Retardation

Pediatric Neurology Briefs

Volume 28 (2014): Issue 11

By: J Gordon Millichap and John J Millichap

Open Access

|Nov 2014

Abstract

Investigators at Universite de Lille Nord de France, and other centers in France, report the identification of a novel causative gene for spinocerebellar ataxia 21, an autosomal dominant disorder, initially mapped to chromosome 7 and designated as SCA21.

References

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Ropper AH Samuels MA Adams and Victor's Principles of Neurology 2009 9th ed New York McGraw Hill Medical 1052
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Huang L Szymanska K Jensen VL Janecke AR Innes AM Davis EE TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone Am J Hum Genet 2011 12 9 89 6 713 30 10.1016/j.ajhg.2011.11.005 22152675
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Articles in this issue

DOI: https://doi.org/10.15844/pedneurbriefs-28-11-1 | Journal eISSN: 2166-6482

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Language: English

Page range: 81 - 82

Published on: Nov 1, 2014

Published by: Pediatric Neurology Briefs Publishers

In partnership with: Paradigm Publishing Services

Keywords:

Neurology,

Pediatrics,

Child Development,

Nervous System Diseases,

Brain Diseases

© 2014 J Gordon Millichap, John J Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.

Volume 28 (2014): Issue 11