Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome - Concepedia

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Publication | Open Access

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

DOI Full Paper Access

850

Citations

10

References

2003

Year

Jeanne Amiel, Béatrice Laudier, Tania Attié‐Bitach, Ha Trang, Loïc de Pontual, Blanca Gener, Delphine Trochet, Heather Etchevers, Pierre F. Ray, Michel Simonneau,

Nature Genetics

Genetic DisorderGeneticsInherited Metabolic DiseaseHypoxia (Medicine)PediatricsPolyalanine ExpansionCongenital Heart AnomalyMedicineFrameshift MutationsSleep Disordered BreathingNeurogenetics

References

	Year	Citations

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