Analysis of Hungarian patients with Rett syndrome phenotype for MECP2, CDKL5 and FOXG1 gene mutations
Bibliographic Information
- Other Title
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- Analysis of Hungarian patients with Rett syndrome phenotype for MECP2 CDKL5 and FOXG1 gene mutations
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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 56 (3), 183-187, 2011-03
Tokyo : Springer Nature
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Keywords
Details 詳細情報について
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- CRID
- 1523388080031234432
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- NII Article ID
- 10030658147
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- NII Book ID
- AA11206160
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- ISSN
- 14345161
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- NDL BIB ID
- 11012729
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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
