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Article

Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with Hirschsprung disease.

American journal of medical genetics. Part A - 1 Jun 2008

Fitze Guido, König Inke R, Paditz Ekkehart, Serra Alexandre, Schläfke Marianne, Roesner Dietmar, Ziegler Andreas, Schackert Hans K

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Identifiers

PMID: 18438890
DOI: 10.1002/ajmg.a.32300

Genes

RET

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Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with Hirschsprung disease.PMID 18438890Read ↗

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PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome.Semantic proximity Read ↗

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