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GATA6 haploinsufficiency causes pancreatic agenesis in humans.

Allen, Hana Lango (author)
Flanagan, Sarah E (author)
Shaw-Smith, Charles (author)
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De Franco, Elisa (author)
Akerman, Ildem (author)
Caswell, Richard (author)
Ferrer, Jorge (author)
Hattersley, Andrew T (author)
Ellard, Sian (author)
Adolfsson, Peter, 1963 (author)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper, Avdelningen för pediatrik,Institute of Clinical Sciences, Department of Pediatrics
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 (creator_code:org_t)
2011-12-11
2012
English.
In: Nature genetics. - : Springer Science and Business Media LLC. - 1546-1718 .- 1061-4036. ; 44:1, s. 20-2
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Understanding the regulation of pancreatic development is key for efforts to develop new regenerative therapeutic approaches for diabetes. Rare mutations in PDX1 and PTF1A can cause pancreatic agenesis, however, most instances of this disorder are of unknown origin. We report de novo heterozygous inactivating mutations in GATA6 in 15/27 (56%) individuals with pancreatic agenesis. These findings define the most common cause of human pancreatic agenesis and establish a key role for the transcription factor GATA6 in human pancreatic development.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Pediatrik (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Pediatrics (hsv//eng)

Keyword

GATA6 Transcription Factor
genetics
Haploinsufficiency
Humans
Pancreas
abnormalities
Phenotype

Publication and Content Type

ref (subject category)
art (subject category)

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