Preskoči na sadržaj
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Napredno
  • The previously reported T342P...
  • Citiraj ovo
  • Pošalji tekstualnu poruku
  • Pošalji ovo e-mailom
  • Ispiši
  • Izvezi zapis
    • Izvezi u RefWorks
    • Izvezi u EndNoteWeb
    • Izvezi u EndNote
  • Stalna poveznica
The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY.

The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY.

Pokaži ostale verzije (1)
Bibliografski detalji
Glavni autori: Steele, A, Tribble, N, Caswell, R, Wensley, K, Hattersley, A, Gloyn, A, Ellard, S
Format: Journal article
Jezik:English
Izdano: 2011
  • Primjerci
  • Opis
  • Ostale verzije (1)
  • Slični predmeti
  • Prikaz za djelatnike knjižnice

Slični predmeti

  • The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY
    od: Steele, A, i dr.
    Izdano: (2011)
  • Insights into the pathogenicity of rare missense GCK variants from the identification and functional characterization of compound heterozygous and double mutations inherited in cis.
    od: Beer, N, i dr.
    Izdano: (2012)
  • Identification of 21 novel glucokinase (GCK) mutations in UK and European Caucasians with maturity-onset diabetes of the young (MODY).
    od: Thomson, K, i dr.
    Izdano: (2003)
  • Identification and functional characterisation of novel inactivating glucokinase mutations causing GCK-MODY in Slovakia
    od: Valentinova, L, i dr.
    Izdano: (2011)
  • Activating glucokinase (GCK) mutations as a cause of medically responsive congenital hyperinsulinism: prevalence in children and characterisation of a novel GCK mutation.
    od: Christesen, H, i dr.
    Izdano: (2008)

Opcije pretrage

  • Povijest pretrage
  • Napredna pretraga

Pronađi više

  • Pregledaj katalog
  • Pregledaj abecednim redom
  • Istraži kanale
  • Rezervacije tečajeva
  • Novi predmeti

Trebaš pomoć?

  • Savjeti za pretragu
  • Upitaj knjižničara
  • Često postavljena pitanja