Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease [published erratum appears in Hum Mol Genet 1998 Oct;7(11):1831]
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収録刊行物
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- Human Molecular Genetics
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Human Molecular Genetics 7 (9), 1449-1452, 1998-09-01
Oxford University Press (OUP)
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詳細情報 詳細情報について
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- CRID
- 1363670320834699776
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- NII論文ID
- 30018400915
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- NII書誌ID
- AA10836720
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- ISSN
- 14602083
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