Bi-allelic Loss-of-Function Variants in DNMBP Cause Infantile Cataracts.

Journal: American Journal of Human Genetics

Published: 2018-10-04

DOI: 10.1016/j.ajhg.2018.09.004

Affiliations: 16

Authors: 21

Go to article
Institutions FC
Department of Genetic Medicine and Development, UNIGE, Switzerland 0.21
Institute of Basic Medical Sciences (IBMS), KMU, Pakistan 0.19
Department of Genetics, University of Karachi, Pakistan 0.17
University Hospital of Geneva (HUG), Switzerland 0.06
Manchester Centre for Genomic Medicine (MCGM), United Kingdom (UK) 0.05
Hirslanden Clinique La Colline, Switzerland 0.05
Division of Evolution and Genomic Sciences, UoM, United Kingdom (UK) 0.05
Neuroscience and Mental Health Domain, UoM, United Kingdom (UK) 0.05
Department of Molecular and Human Genetics, BCM, United States of America (USA) 0.04
Jan and Dan Duncan Neurological Research Institute at Texas Children's Hospital (NRI), United States of America (USA) 0.04
Biomedical Research Foundation (BRFAA), Academy of Athens, Greece 0.02
University Hospital of Lausanne (CHUV), UNIL, Switzerland 0.02
Department of Bio Sciences, Mohammad Ali Jinnah University, Pakistan 0.02
Institute of Genetics and Genomics in Geneva (iGE3), UNIGE, Switzerland 0.02
Program in Developmental Biology, BCM, United States of America (USA) 0.02
Howard Hughes Medical Institute (HHMI), United States of America (USA) 0

Return