Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse)

Author： de Pontual Loïc  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.12, Iss.23, 2003-12, pp. : 3173-3180

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Distinct pathogenetic mechanisms for PHOX2B associated polyalanine expansions and frameshift mutations in congenital central hypoventilation syndrome

By Bachetti Tiziana   Matera Ivana   Borghini Silvia   Duca Marco Di   Ravazzolo Roberto   Ceccherini Isabella  

Human Molecular Genetics, Vol. 14, Iss. 13, 2005-07 ,pp. : 1815-1824

Oxford University Press

Access to resources Recommend Favorite

Homozygous Mutation of the FGFR1 Gene Associated with Congenital Heart Disease and 46,XY Disorder of Sex Development

By  

Sexual Development, Vol. 10, Iss. 1, 2016-04 ,pp. : 16-22

Karger

Access to resources Recommend Favorite

Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome

By Cross Sally H.  

Human Molecular Genetics, Vol. 13, Iss. 14, 2004-07 ,pp. : 1433-1439

Oxford University Press

Access to resources Recommend Favorite

Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome

By Semina E.V.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1113-1117

Oxford University Press

Access to resources Recommend Favorite

Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1

By Mee Lisa  

Human Molecular Genetics, Vol. 14, Iss. 11, 2005-06 ,pp. : 1475-1488

Oxford University Press

Access to resources Recommend Favorite