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Paper Title
Rare Noncoding Mutations Extend the Mutational Spectrum in the PGAP3 Subtype of Hyperphosphatasia with Mental Retardation Syndrome.
PubMed
Paper Journal Title
Hum Mutat
Paper Citation Count
37
Paper Publication Year
2016
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Author Name
Affiliation
Ingo Helbig
The Children's Hospital of Philadelphia
Ingo Helbig
University Medical Center Schleswig-Holstein
Michal R Schweiger
University of Cologne
Peter N Robinson
Institute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Peter N Robinson
Max Planck Institute for Molecular Genetics
Peter N Robinson
Institute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Peter N Robinson
Max Planck Institute for Molecular Genetics
Stefan Mundlos
Institute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Stefan Mundlos
Max Planck Institute for Molecular Genetics
Denise Horn
Institute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Peter M Krawitz
Institute for Medical and Human Genetics, Charite-Universitatsmedizin Berlin
Peter M Krawitz
Max Planck Institute for Molecular Genetics
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