Title : Extreme intra-familial variability of congenital central hypoventilation syndrome: a case series.

Pub. Date : 2013 Apr 26

PMID : 23622117






1 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 Most cases are caused by polyalanine repeat mutations in the paired-like homeobox 2B gene, PHOX2B. polyalanine paired like homeobox 2B Homo sapiens