DCDC2Mutations Cause Neonatal Sclerosing Cholangitis-Reference-Cited by-同舟云学术

DCDC2Mutations Cause Neonatal Sclerosing Cholangitis

Published:2016-08-24 Issue:10 Volume:37 Page:1025-1029
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Girard Muriel¹²³,Bizet Albane A.²⁴,Lachaux Alain⁵⁶,Gonzales Emmanuel⁷⁸,Filhol Emilie²⁴,Collardeau-Frachon Sophie⁶⁹,Jeanpierre Cécile²⁴,Henry Charline²⁴,Fabre Monique¹⁰,Viremouneix Loic¹¹⁶,Galmiche Louise¹⁰,Debray Dominique¹,Bole-Feysot Christine¹²,Nitschke Patrick¹³,Pariente Danièle¹⁴⁸,Guettier Catherine¹⁵⁸,Lyonnet Stanislas²³,Heidet Laurence²⁴,Bertholet Aurelia¹⁶⁶,Jacquemin Emmanuel⁷⁸,Henrion-Caude Alexandra²,Saunier Sophie²⁴

Affiliation:

1. Hepatology Unit; Necker Hospital; Assistance Publique-Hopitaux de Paris; France

2. Paris Descartes Sorbonne Paris Cité University; Imagine institute; Paris France

3. Inserm UMR-1163; Laboratory of Embryology and Genetics of Human Malformations; Paris France

4. Inserm UMR-1163; Laboratory of Hereditary Kidney Diseases; Paris France

5. Service d'Hépatologie; Gastroentérologie et Nutrition Pédiatriques; Hôpital Femme-Mère-Enfant; Hospices Civils de Lyon Bron France

6. Université Claude Bernard Lyon 1; Lyon France

7. Pediatric Hepatology and Liver Transplantation Unit; Reference Centre for Pediatric Liver Diseases, Bicêtre Hospital; Assistance Publique-Hôpitaux de Paris; France

8. Université Paris-Sud 11; France

9. Service de Pathologie; Groupement Hospitalier Est; Hospices Civils de Lyon; Bron France

10. Pathology Department; Necker Hospital; Assistance Publique-Hôpitaux de Paris; France

11. Hospices Civils de Lyon; Département D'imagerie Digestive; Hôpital E. Herriot; Lyon France

12. Inserm UMR-1163; Genomic Core Facility; Paris France

13. Inserm UMR-1163; Bioinformatic Core Facility; Paris France

14. Department of Pediatric Radiology; Bicêtre Hospital; Le Kremlin-Bicêtre France

15. Service d'Anatomopathologie; AP-HP Hôpital Kremlin-Bicêtre; Paris France

16. Néphrogones; Centre de Référence des Maladies Rénales Rares; Hospices Civils de Lyon; Bron France

Funder

GIS-Institut des Maladies Rares

Fondation pour la Recherche Médicale

Foundation GIS-Maladies Rares

European Union's Seventh Framework Program

EURenOmics

Fondation ARC pour la Recherche sur le Cancer

ANR

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization;Bizet;Nat Commun,2015

2. Common and divergent roles for members of the mouse DCX superfamily;Coquelle;Cell Cycle,2006

3. Three dyslexia susceptibility genes, DYX1C1, DCDC2, and KIAA0319, affect temporo-parietal white matter structure;Darki;Biol Psychiatry,2012

4. Sclerosing cholangitis in children;Debray;J Pediatr,1994

5. Mutation of the dyslexia-associated gene Dcdc2 impairs LTM and visuo-spatial performance in mice;Gabel;Genes Brain Behav,2011

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