Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort-Reference-Cited by-同舟云学术

Novel C2orf71 mutations account for ∼1% of cases in a large French arRP cohort

Published:2011-02-08 Issue:4 Volume:32 Page:
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Audo Isabelle¹²³⁴⁵,Lancelot Marie‐Elise¹²³,Mohand‐Saïd Saddek¹²³⁴,Antonio Aline¹²³⁴,Germain Aurore¹²³,Sahel José‐Alain¹²³⁴⁵,Bhattacharya Shomi S¹²³⁵⁶,Zeitz Christina¹²³

Affiliation:

1. INSERM, U968, Paris, F‐75012, France

2. CNRS, UMR_7210, Paris, F‐75012, France

3. UPMC Univ Paris 06, UMR_S 968, Department of Genetics, Institut de la Vision, Paris, F‐75012, France

4. Centre Hospitalier National d'Ophtalmologie des Quinze‐Vingts, INSERM‐DHOS CIC 503, Paris, F‐75012, France

5. Department of Molecular Genetics, Institute of Ophthalmology, London, UK

6. Unidad Clínica de Genética, Reproducción y Medicina Fetal. Hospital Universitario Virgen del Rocío, Seville, Spain, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Seville, Spain

Funder

Agence Nationale de la Recherche

Foundation Voir et Entendre

Foundation Fighting Blindness

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/humu.21460

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