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

Kwon, Kyoung-Ah

A case of congenital central hypoventilation syndrome with PHOX2B gene mutation in a Korean neonate. [electronic resource] - Journal of Korean medical science Aug 2010 - 1237-40 p. digital

Publication Type: Case Reports; Journal Article

1598-6357

10.3346/jkms.2010.25.8.1237 doi


Alleles
Asian People--genetics
Genotype
Homeodomain Proteins--genetics
Humans
Hypoventilation--congenital
Infant, Newborn
Male
Mutation
Peptides--genetics
Republic of Korea
Sequence Analysis, DNA
Transcription Factors--genetics
Ventilators, Mechanical