Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome-Reference-Cited by-同舟云学术

Transcriptional dysregulation and impairment of PHOX2B auto-regulatory mechanism induced by polyalanine expansion mutations associated with congenital central hypoventilation syndrome

Published:2013-02 Issue: Volume:50 Page:187-200
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Di Lascio Simona,Bachetti Tiziana,Saba Elena,Ceccherini Isabella,Benfante Roberta,Fornasari Diego

Funder

Fondazione Cariplo

Fondazione Mariani

Italian Ministry of Health

Italian Ministry of University Research

University of Milan

Publisher

Elsevier BV

Subject

Neurology

Reference43 articles.

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3. A molecular pathogenesis for transcription factor associated poly-alanine tract expansions;Albrecht;Hum. Mol. Genet.,2004

4. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat. Genet.,2003

5. Polyalanine expansions in human;Amiel;Hum. Mol. Genet.,2004

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