MECP2 Mutations in Sporadic Cases of Rett Syndrome Are Almost Exclusively of Paternal Origin
収録刊行物
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- The American Journal of Human Genetics
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The American Journal of Human Genetics 68 (5), 1093-1101, 2001-05
Elsevier BV
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詳細情報 詳細情報について
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- CRID
- 1362262945076360064
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- NII論文ID
- 30017635255
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- DOI
- 10.1086/320109
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- ISSN
- 00029297
- http://id.crossref.org/issn/00029297
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- データソース種別
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- Crossref
- CiNii Articles