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雑誌Journal of human genetics
Volume number60(4):2015.4
ArticleA Japanese...

A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation

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A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation

Call No. (NDL)
Z54-H248
Bibliographic ID of National Diet Library
026332543
Material type
記事
Author
Misako Kuniiほか
Publisher
Tokyo : Springer Nature
Publication date
2015-04
Material Format
Paper
Journal name
Journal of human genetics / Japan Society of Human Genetics 60(4):2015.4
Publication Page
p.187-191
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Paper

Material Type
記事
Title
A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation
Author/Editor
Misako Kunii
Hiroshi Doi
Yuichi Higashiyama 他
Author Heading
Misako Kunii
Hiroshi Doi
Yuichi Higashiyama
Periodical title
Journal of human genetics / Japan Society of Human Genetics
No. or year of volume/issue
60(4):2015.4
Volume
60
Issue
4
Pages
187-191
Publication date of volume/issue (W3CDTF)
2015-04