Hypertriglyceridemia as a main feature associated with 17q12 deletion syndrome-related hepatocyte nuclear factor 1β-maturity-onset diabetes of the young

SUMMARY: Hepatocyte nuclear factor 1β (HNF1B) gene is located on chromosome 17q12. It is a transcription factor implicated in the early embryonic development of multiple organs. HNF1B-associated disease is a multi-system disorder with variable clinical phenotypes. There are increasing reports sugges...

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Detalles Bibliográficos
Autores principales: Thewjitcharoen, Yotsapon, Nakasatien, Soontaree, Tsoi, Tsz Fung, Lim, Cadmon K P, Himathongkam, Thep, Chan, Juliana C N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2022
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513634/
https://www.ncbi.nlm.nih.gov/pubmed/36106561
http://dx.doi.org/10.1530/EDM-22-0297

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9513634/
https://www.ncbi.nlm.nih.gov/pubmed/36106561
http://dx.doi.org/10.1530/EDM-22-0297

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