Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome.
Meguro T; Yoshida Y; Hayashi M; Toyota K; Otagiri T; Mochizuki N; Kishikawa Y; Sasaki A; Hayasaka K; Journal Of Human Genetics, 2012, vol. 57, issue 5, p 335, ISSN 1435232x. ISBN 1435232x.

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