Genetic variants in ESRRG are associated with a dominant non-progressive congenital movement disorder with ataxia

Journal:

American Journal of Human Genetics

Published:

2025-11-19

DOI:

10.1016/j.ajhg.2025.10.015

Affiliations:

11

Authors:

19

Go to article

Institutions	Authors	Share
Universitätsklinikum Leipzig, Germany	4.000000	0.21
Amsterdam UMC, Netherlands	3.000000	0.16
Assistance Publique-Hôpitaux de Paris (AP-HP), France	2.000000	0.11
Baylor College of Medicine (BCM), United States of America (USA)	2.000000	0.11
Centogene AG, Germany	2.000000	0.11
Hospital Timone, France	1.000000	0.05
AP-HP Pitié-Salpêtrière Hospital, France	1.000000	0.05
Izmir Kâtip Celebi University, Turkey	1.000000	0.05
Hôpital Roger Salengro, France	1.000000	0.05
Sozialpädiatrisches Zentrum Frankfurt Mitte (SPZ Frankfurt Mitte), Germany	1.000000	0.05
University of Erlangen-Nuremberg (FAU), Germany	1.000000	0.05

Interested in Genetics?