A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting as central sleep apnea.
Amimoto Y, Okada K, Nakano H, Sasaki A, Hayasaka K, Odajima H.
Amimoto Y, et al. Among authors: odajima h.
J Clin Sleep Med. 2014 Mar 15;10(3):327-9. doi: 10.5664/jcsm.3542.
J Clin Sleep Med. 2014.
PMID: 24634632
Free PMC article.
This mutation is considered to be associated with a relatively mild phenotype. CITATION: Amimoto Y; Okada K; Nakano H; Sasaki A; Hayasaka K; Odajima H. A case of congenital central hypoventilation syndrome with a novel mutation of the PHOX2B gene presenting a …
This mutation is considered to be associated with a relatively mild phenotype. CITATION: Amimoto Y; Okada K; Nakano H; Sasaki A; Haya …