Elucidating the clinical spectrum and molecular basis of HYAL2 deficiency is a research paper published in Genetics in Medicine (2021). On theSindex it has a DataRank of 0. It has been cited 4 times.
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Medical Research Council
Grant: MC_PC_15047
Precision Medicine Exeter Innovation Platform (PMEI Platform): Proof of Concept Funds
Medical Research Council
Grant: MC_PC_15054
Precision Medicine Exeter Innovation Platform (PMEI Platform)
NCATS NIH HHS
Grant: TL1 TR001880
NHGRI NIH HHS
Grant: U01 HG011758
Medical Research Council
Grant: MC_PC_18047
NHGRI NIH HHS
Grant: UM1 HG006542
National Institute for Health Research (NIHR)
Grant: ACF-2018-23-003
Medical Research Council
Grant: G1002279
Accelerated Discovery of Molecules and Biological Pathways Perturbed in Mendelian Neurological Diseases
NHGRI NIH HHS
Grant: K08 HG008986
Medical Research Council
Grant: G1001931
Investigation of the molecular aspects of growth and development
Wellcome Trust
Grant: 220600/Z/20/Z
European Commission
Grant: 779257
Solving the unsolved Rare Diseases
Wellcome Trust
Grant: 220600
Clinical and molecular delineation of neurodevelopmental disease within genetically isolated communities.
National Institutes of Health
Grant: 5TL1TR001880-02
Institutional Clinical and Translational Science Award
National Institutes of Health
Grant: 5K08HG008986-04
Individual genomic analyses to discover the molecular basis and mechanisms contributing to adult-onset disease
National Institutes of Health
Grant: 3UM1HG006542-05S1
Baylor Johns Hopkins Center for Mendelian Genetics
Wellcome Trust
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Sustainable Development Goals