Back to Search
Start Over
ABCC9-related Intellectual disability Myopathy Syndrome is a KATP channelopathy with loss-of-function mutations in ABCC9
- Authors :
- Genetica Groep Van Haaften
Genetica Sectie Genoomdiagnostiek
Child Health
Medische Fysiologie
Circulatory Health
CMM Sectie Genomics and Bioinformatics
Cancer
Smeland, Marie F
McClenaghan, Conor
Roessler, Helen I
Savelberg, Sanne
Hansen, Geir Åsmund Myge
Hjellnes, Helene
Arntzen, Kjell Arne
Müller, Kai Ivar
Dybesland, Andreas Rosenberger
Harter, Theresa
Sala-Rabanal, Monica
Emfinger, Chris H
Huang, Yan
Singareddy, Soma S
Gunn, Jamie
Wozniak, David F
Kovacs, Attila
Massink, Maarten
Tessadori, Federico
Kamel, Sarah M
Bakkers, Jeroen
Remedi, Maria S
Van Ghelue, Marijke
Nichols, Colin G
van Haaften, Gijs
Genetica Groep Van Haaften
Genetica Sectie Genoomdiagnostiek
Child Health
Medische Fysiologie
Circulatory Health
CMM Sectie Genomics and Bioinformatics
Cancer
Smeland, Marie F
McClenaghan, Conor
Roessler, Helen I
Savelberg, Sanne
Hansen, Geir Åsmund Myge
Hjellnes, Helene
Arntzen, Kjell Arne
Müller, Kai Ivar
Dybesland, Andreas Rosenberger
Harter, Theresa
Sala-Rabanal, Monica
Emfinger, Chris H
Huang, Yan
Singareddy, Soma S
Gunn, Jamie
Wozniak, David F
Kovacs, Attila
Massink, Maarten
Tessadori, Federico
Kamel, Sarah M
Bakkers, Jeroen
Remedi, Maria S
Van Ghelue, Marijke
Nichols, Colin G
van Haaften, Gijs
- Publication Year :
- 2019
Details
- Database :
- OAIster
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1432111693
- Document Type :
- Electronic Resource