Title : Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

Pub. Date : 2012 Jul

PMID : 23723037






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 CCHS is characterized by lack of ventilatory chemosensitivity caused by PHOX2B gene abnormalities consisting mainly of alanine expansions. Alanine paired-like homeobox 2b Mus musculus