The patient-specific mouse model with frameshift mutation provides insights into the pathophysiology of FOXG1 syndrome

Journal:

Nature Communications

Published:

2025-05-22

DOI:

10.1038/s41467-025-59838-4

Affiliations:

8

Authors:

12

Go to article

Institutions	Authors	Share
University at Buffalo, The State University of New York (SUNY UB), United States of America (USA)	9.333333	0.78
Sungkyunkwan University (SKKU), South Korea	1.000000	0.08
FOXG1 Research Foundation, United States of America (USA)	0.500000	0.04
Citizen Health, United States of America (USA)	0.500000	0.04
University of Pennsylvania (Penn), United States of America (USA)	0.333333	0.03
Samsung Medical Center (SMC), South Korea	0.333333	0.03

Interested in Genetics?