Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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The integrative role of the sigh in psychology, physiology, pathology, and neurobiology.Neural Control of the Upper Airway: Respiratory and State-Dependent Mechanisms.Inflammatory lung disease in Rett syndrome.Facing the challenge of mammalian neural microcircuits: taking a few breaths may help.

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P2860

Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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P1476

Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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Jorge Gallego

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SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

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

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region

Rett syndrome: revised diagnostic criteria and nomenclature

NTNG1 mutations are a rare cause of Rett syndrome

MeCP2, a key contributor to neurological disease, activates and represses transcription

The common BDNF polymorphism may be a modifier of disease severity in Rett syndrome

Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

Rett syndrome: clinical review and genetic update

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2255-2279

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scholarly article

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10.1002/CPHY.C100037

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2012-07-01T00:00:00Z

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23723037

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P921

birth defect

Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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P2860

P2860

Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.

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P1476

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P921