Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy-Reference-Cited by-同舟云学术

Dominant mutations in mtDNA maintenance gene SSBP1 cause optic atrophy and foveopathy

Published:2019-11-18 Issue:1 Volume:130 Page:143-156
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Piro-Mégy Camille,Sarzi Emmanuelle,Tarrés-Solé Aleix^ORCID,Péquignot Marie,Hensen Fenna,Quilès Mélanie,Manes Gaël^ORCID,Chakraborty Arka^ORCID,Sénéchal Audrey,Bocquet Béatrice^ORCID,Cazevieille Chantal,Roubertie Agathe,Müller Agnès,Charif Majida,Goudenège David^ORCID,Lenaers Guy^ORCID,Wilhelm Helmut,Kellner Ulrich^ORCID,Weisschuh Nicole^ORCID,Wissinger Bernd^ORCID,Zanlonghi Xavier,Hamel Christian,Spelbrink Johannes N.^ORCID,Sola Maria,Delettre Cécile

Funder

Institut National de la Santé et de la Recherche Médicale

University of Montpellier

Union National des Aveugles et Déficients Visuels UNADEV

Spanish Ministry of Science

MINECO

European Union

Prinses Beatrix Spierfonds and the Stichting Spieren voor Spieren

Publisher

American Society for Clinical Investigation

Subject

General Medicine