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Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype–phenotype correlation in congenital central hypoventilation syndrome (CCHS)

Paired-like Homeobox GeneMendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyPediatricsGenotype–phenotype CorrelationMedical GeneticsMedicineRepeat Expansion MutationsSleep Disordered Breathing