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Q48273157-08DBB063-81E1-4A31-A98E-65D8A0E159C7
Q48273157-08DBB063-81E1-4A31-A98E-65D8A0E159C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48273157-08DBB063-81E1-4A31-A98E-65D8A0E159C7
Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.
P2860
Q48273157-08DBB063-81E1-4A31-A98E-65D8A0E159C7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48273157-08DBB063-81E1-4A31-A98E-65D8A0E159C7
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type
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wasDerivedFrom
3d60844cc233d371f410b9514fe4450000cd24a8
P2860
Congenital central hypoventilation syndrome: PHOX2B mutations and phenotype.