Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity-Reference-Cited by-同舟云学术

Homozygosity Mapping of Portuguese and Japanese Forms of Ataxia-Oculomotor Apraxia to 9p13, and Evidence for Genetic Heterogeneity

Published:2001-02 Issue:2 Volume:68 Page:501-508
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Moreira Maria do Céu,Barbot Clara,Tachi Nobutada,Kozuka Naoki,Mendonça Pedro,Barros José,Coutinho Paula,Sequeiros Jorge,Koenig Michel

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference21 articles.

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3. A variant type of early onset spinocerebellar degeneration with ocular motor apraxia and choreoathetosis;Awaya;Jpn J Pediatr,1985

4. A hereditary variant of spinocerebellar degeneration associated with choreoathetosis and ocular motor apraxia of early onset;Awaya;Acta Paediatr Jpn,1986

5. Barbot C, Coutinho P, Chorao R, Ferreira C, Barros J, Fineza I, Dias K, Monteiro JP, Guimarães A, Mendonça P, Moreira MC, Sequeiros J. Recessive ataxia with ocular apraxia: review of 22 Portuguese patients. Arch Neurol (in press)

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