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Homogentisate 1,2-dioxygenase (HGD) gene variants causing alkaptonuria (AKU) in different countries and increased mutation frequency in a specific region of Slovakia

  1. TitleHomogentisate 1,2-dioxygenase (HGD) gene variants causing alkaptonuria (AKU) in different countries and increased mutation frequency in a specific region of Slovakia
    Author Kádaši Ľudevít 1952- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV    ORCID
    Co-authors Radvánszky Ján 1982- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV

    Gallagher James A.

    Jarvis Jonathan C.

    Ranganath Lakshminarayan R.

    Usher Jeannette L.

    Alsbou Mohammed S.

    Zaťková Andrea 1971- SAVMOFYZ - Ústav molekulárnej fyziológie a genetiky SAV    SCOPUS    RID    ORCID

    Source document Genomic Disorders 2011: The Genomics of Rare Diseases : 23-26 March 2011. P. 11. - Cambridge, 2011 ; Genomic Disorders 2011: The Genomics of Rare Diseases
    Languageeng - English
    Document kindrozpis článkov z periodík (rzb)
    CategoryAFG - Abstracts of papers from foreign conferences
    Year2011
    article

    article

    rok vydaniarok metrikyIFIF Q (best)SJRSJR Q (best)
    2011
Number of the records: 1  

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