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Paper Details

Behr syndrome and hypertrophic cardiomyopathy in a family with a novel UCHL1 deletion.
J Neurol
7
2020
Author NameAffiliation
Hanns Lochm??llerMedical Center - University of Freiburg
Hanns Lochm??llerCenter for Genomic Regulation, Barcelona Institute of Science and Technology (BIST)
Hanns Lochm??llerChildren's Hospital of Eastern Ontario Research Institute, The Ottawa Hospital and Brain and Mind Research Institute, University of Ottawa
Patrick F ChinneryUniversity of Cambridge School of Clinical Medicine
Patrick F ChinneryUniversity of Cambridge
Sergi BeltranCenter for Genomic Regulation, Barcelona Institute of Science and Technology (BIST)
Leslie MatalongaCenter for Genomic Regulation, Barcelona Institute of Science and Technology (BIST)
Rita HorvathUniversity of Cambridge School of Clinical Medicine
Rita HorvathUniversity of Cambridge School of Clinical Medicine
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