Genotype–phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia-Reference-Cited by-同舟云学术

Genotype–phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemia

Published:2011-04-12 Issue:5 Volume:134 Page:1387-1399
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Yokoseki Akio,Ishihara Tomohiko,Koyama Akihide,Shiga Atsushi,Yamada Mitsunori,Suzuki Chieko,Sekijima Yoshiki,Maruta Kyoko,Tsuchiya Miyuki,Date Hidetoshi,Sato Tatsuya,Tada Masayoshi,Ikeuchi Takeshi,Tsuji Shoji,Nishizawa Masatoyo,Onodera Osamu

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/134/5/1387/13794858/awr069.pdf

Reference29 articles.

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3. Aprataxin gene mutations in Tunisian families;Amouri;Neurology,2004

4. A case of congenital ocular motor apraxia with cerebellospinal degeneration;Araie;Jpn J Opthalmol,1977

5. Recessive ataxia with ocular apraxia: review of 22 Portuguese patients;Barbot;Arch Neurol,2001

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