- A novel HNF4A mutation c. 427-1G A causing congenital hyperinsulinism…
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A novel HNF4A mutation c. 427-1G A causing congenital hyperinsulinism and glycogenosis - like phenotype

  1. TitleA novel HNF4A mutation c. 427-1G A causing congenital hyperinsulinism and glycogenosis - like phenotype
    Author Staník Juraj SAVBIOMED - Biomedicínske centrum SAV
    Co-authors Škopková Martina SAVBIOMED - Biomedicínske centrum SAV
    Brennerová Katarína
    Daniš Daniel 1989 SAVBIOMED - Biomedicínske centrum SAV
    Rosoľanková Monika
    Salingova Anna
    Bzduch Vladimir
    Klimeš Iwar SAVBIOMED - Biomedicínske centrum SAV
    Gašperíková Daniela SAVBIOMED - Biomedicínske centrum SAV
    Action APVV-0107-12. Molekulárno-genetický výskum s farmakogenetickými konsekvenciami u detí s hyperinzulinemickými hypoglykémiami : 2013-2017 : BMC-ÚEE
    Source document Genetics of diabetes and its role in precision medicine : 6th EASD - SGGD meeting. P. 120. - Leiden : Leiden University Medical Center, 2017 ; EASD - SGGD meeting Genetics of diabetes and its role in precision medicine
    CategoryGII - Other publications and documents which is not possible to categorize into classes/categories mentioned above
    Year2017
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Number of the records: 1  

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