Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome-Reference-Cited by-同舟云学术

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

Published:2003-03-17 Issue:4 Volume:33 Page:459-461
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Amiel Jeanne,Laudier Béatrice,Attié-Bitach Tania,Trang Ha,de Pontual Loïc,Gener Blanca,Trochet Delphine,Etchevers Heather,Ray Pierre,Simonneau Michel,Vekemans Michel,Munnich Arnold,Gaultier Claude,Lyonnet Stanislas

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1130.pdf

Reference15 articles.

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4. Weese-Mayer, D.E., Silvestri, J.M., Marazita, M.L. & Hoo, J.J. Am. J. Med. Genet. 47, 360–367 (1993).

5. Amiel, J. et al. Am. J. Hum. Genet. 62, 715–717 (1998).

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