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PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.

Chinese medical journal - 20 Oct 2006

Or Siu-Fong June, Tong Ming-for Tony, Lo Fai-Man Ivan, Law Chi-Wai, Miu Ting-Yat, Trochet Delphine, Lam Tak-Sum Stephen

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PMID: 17097025

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Related research

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PHOX2B mutations in three Chinese patients with congenital central hypoventilation syndrome.PMID 17097025Read ↗

Congenital central hypoventilation syndrome due to PHOX2B mutation in a Saudi child: a case report.Semantic proximity Read ↗

Genetic study of a patient with congenital central hypoventilation syndrome in Iran: a case report.Semantic proximity Read ↗

Adult With PHOX2B Mutation and Late-Onset Congenital Central Hypoventilation SyndromeSemantic proximity Read ↗

Genetic study of apatient with congenital central hypoventilation syndrome in Iran: a case reportSemantic proximity Read ↗

<i>PHOX2B</i> mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndromeSemantic proximity Read ↗

PHOX2B gene mutation in a patient with late-onset central hypoventilation.Semantic proximity Read ↗

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

Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome.Semantic proximity Read ↗

Late-onset, insidious course and invasive treatment of congenital central hypoventilation syndrome in a case with the Phox2B mutation: case report.Semantic proximity Read ↗

A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate.Semantic proximity Read ↗

PHOX2B mutation in a Taiwanese newborn with congenital central hypoventilation syndrome.Semantic proximity Read ↗

Significant phenotype variability of congenital central hypoventilation syndrome in a family with polyalanine expansion mutation of the PHOX2B gene.Semantic proximity Read ↗

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