PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

• MATERA I

収録刊行物

• J Med Genet

  J Med Genet 41 373-380, 2004

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• CRID: 1572543025454554368
• NII論文ID: 10021249512
• データソース種別:
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