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Sökning: onr:"swepub:oai:lup.lub.lu.se:6a0a638a-5e30-4ff9-ba97-13f6e8cfe784" > Recognition of matu...

  • Liang, HuaThird Affiliated Hospital of Sun Yat‐sen University (författare)

Recognition of maturity-onset diabetes of the young in China

  • Artikel/kapitelEngelska2021

Förlag, utgivningsår, omfång ...

  • 2020-09-09
  • Wiley,2021

Nummerbeteckningar

  • LIBRIS-ID:oai:lup.lub.lu.se:6a0a638a-5e30-4ff9-ba97-13f6e8cfe784
  • https://lup.lub.lu.se/record/6a0a638a-5e30-4ff9-ba97-13f6e8cfe784URI
  • https://doi.org/10.1111/jdi.13378DOI

Kompletterande språkuppgifter

  • Språk:engelska
  • Sammanfattning på:engelska

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Klassifikation

  • Ämneskategori:art swepub-publicationtype
  • Ämneskategori:ref swepub-contenttype

Anmärkningar

  • Aims/Introduction: Given that mutations related to maturity-onset diabetes of the young (MODY) are rarely found in Chinese populations, we aim to characterize the mutation spectrum of MODY pedigrees. Materials and Methods: Maturity-onset diabetes of the young candidate gene- or exome-targeted capture sequencing was carried out in 76 probands from unrelated families fulfilling the clinical diagnostic criteria for MODY. MAF <0.01 in the GnomAD or ExAC database was used to filter significant variants. Sanger sequencing was then carried out to validate findings. Function prediction by SIFT, PolyPhen-2 and PROVEAN or CADD was carried out in missense mutations. Results: A total of 32 mutations in six genes were identified in 31 families, accounting for 40.79% of the potential MODY families. The MODY subtype detection rate was 18.42% for GCK, 15.79% for HNF1A, 2.63% for HNF4A, and 1.32% for KLF11, PAX4 and NEUROG3. Seven nonsense/frameshift mutations and four missense mutations with damaging prediction were newly identified novel mutations. The clinical features of MODY2, MODY3/1 and MODYX are similar to previous reports. Clinical phenotype of NEUROG3 p.Arg55Glufs*23 is characterized by hyperglycemia and mild intermittent abdominal pain. Conclusions: This study adds to the emerging pattern of MODY epidemiology that the proportion of MODY explained by known pathogenic genes is higher than that previously reported, and found NEUROG3 as a new causative gene for MODY.

Ämnesord och genrebeteckningar

Biuppslag (personer, institutioner, konferenser, titlar ...)

  • Zhang, YananThird Affiliated Hospital of Sun Yat‐sen University (författare)
  • Li, MaixinyueNanning Children’s Hospital (författare)
  • Yan, JinhuaThird Affiliated Hospital of Sun Yat‐sen University (författare)
  • Yang, DaizhiThird Affiliated Hospital of Sun Yat‐sen University (författare)
  • Luo, SihuiUniversity of Science and Technology of China (författare)
  • Zheng, XueyingUniversity of Science and Technology of China (författare)
  • Yang, GuoqingGeneral Hospital of People's Liberation Army (författare)
  • Li, ZhuoThird Affiliated Hospital of Sun Yat‐sen University (författare)
  • Xu, WenThird Affiliated Hospital of Sun Yat‐sen University (författare)
  • Groop, LeifLund University,Lunds universitet,Translationell muskelforskning,Forskargrupper vid Lunds universitet,Translational Muscle Research,Lund University Research Groups(Swepub:lu)endo-lgr (författare)
  • Weng, JianpingThird Affiliated Hospital of Sun Yat‐sen University (författare)
  • Third Affiliated Hospital of Sun Yat‐sen UniversityNanning Children’s Hospital (creator_code:org_t)

Sammanhörande titlar

  • Ingår i:Journal of Diabetes Investigation: Wiley12:4, s. 501-5092040-11162040-1124

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