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Paper Details

PDE3A mutations cause autosomal dominant hypertension with brachydactyly.
Nat Genet
111
2015
Author NameAffiliation
Herbert Schulz1] Max Delbruck Center for Molecular Medicine in the Helmholtz Association (MDC), Germany. [2] Cologne Center for Genomics (CCG), University of Cologne
Peter M Krawitz1] Max Planck Institute for Molecular Genetics, Germany. [2] Institute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin, Germany. [3] Berlin Brandenburg Center for Regenerative Therapies (BCRT)
Jochen Hecht1] Max Planck Institute for Molecular Genetics, Germany. [2] Berlin Brandenburg Center for Regenerative Therapies (BCRT), Charite Universitatsmedizin Berlin
Norbert H??bner1] Max Delbruck Center for Molecular Medicine in the Helmholtz Association (MDC), Germany. [3] Charite Universitatsmedizin
Norbert H??bner1] Max Delbruck Center for Molecular Medicine in the Helmholtz Association (MDC), Germany. [3] Charite Universitatsmedizin
Stefan Mundlos1] Max Planck Institute for Molecular Genetics, Germany. [2] Institute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin, Germany. [3] Berlin Brandenburg Center for Regenerative Therapies (BCRT)
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