Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions
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Journal
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- Journal of human genetics / Japan Society of Human Genetics
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Journal of human genetics / Japan Society of Human Genetics 57 (5), 338-341, 2012-05
Tokyo : Springer Nature
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Keywords
Details 詳細情報について
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- CRID
- 1522825130793416576
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- NII Article ID
- 10030663240
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- NII Book ID
- AA11206160
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- ISSN
- 14345161
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- NDL BIB ID
- 023661554
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- Text Lang
- en
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- NDL Source Classification
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- ZS16(科学技術--医学--人類遺伝学)
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- Data Source
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- NDL
- CiNii Articles