Solving the unsolved rare diseases in Europe
Eur J Hum Genet
.
2021 Sep;29(9):1319-1320.
doi: 10.1038/s41431-021-00924-8.
Authors
Holm Graessner
1
2
,
Birte Zurek
3
,
Alexander Hoischen
4
5
6
,
Sergi Beltran
7
8
9
Affiliations
1
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
[email protected]
.
2
Centre for Rare Diseases, University Hospital Tübingen, Tübingen, Germany.
[email protected]
.
3
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
4
Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
5
Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
6
Department of Internal Medicine and Radboud Center for Infectious Diseases (RCI), Radboud University Medical Center, Nijmegen, the Netherlands.
7
CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Barcelona, Spain.
8
Universitat Pompeu Fabra (UPF), Barcelona, Spain.
9
Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia, Universitat de Barcelona (UB), Barcelona, Spain.
PMID:
34140650
PMCID:
PMC8440595
DOI:
10.1038/s41431-021-00924-8
No abstract available
Publication types
Editorial
Introductory Journal Article
MeSH terms
Europe
Genetic Diseases, Inborn / diagnosis
Genetic Diseases, Inborn / genetics*
Genetic Testing
Humans
Rare Diseases / diagnosis
Rare Diseases / genetics*