Number of the records: 1  

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 ; SAVEXEND - Biomedicínske centrum SAV
    Co-authors Škopková Martina SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV

    Brennerová Katarína

    Daniš Daniel 1989 SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV

    Rosoľanková Monika

    Salingova Anna

    Bzduch Vladimir

    Klimeš Iwar SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV

    Gašperíková Daniela SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV    RID    ORCID

    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
    Languageeng - English
    CountryNL - Netherlands
    Document kindrozpis článkov z periodík (rzb)
    CategoryGII - Other publications and documents which is not possible to categorize into classes/categories mentioned above
    Year2017
    article

    article

    rok vydaniarok metrikyIFIF Q (best)SJRSJR Q (best)
    2017
Number of the records: 1  

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