Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jonathan Ahern"'
Publikováno v:
Behavior Genetics. 53:292-309
Publikováno v:
Monday, April 24.
Autor:
Robert Loughnan, Jonathan Ahern, Mary Boyle, Terry L. Jernigan, Donald J. Hagler, John R. Iversen, Oleksandr Frei, Diana M. Smith, Ole Andreassen, Leo Sugrue, Wesley K. Thompson, Anders Dale, Andrew J. Schork, Chun Chieh Fan
Iron is an important element required for the body to function properly; however, hemochromatosis, an excess of iron in healthy tissue, can lead to cell damage. C282Y is a genetic variant prevalent in European populations, which is known to increase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f196d5ab18c886cd6ac25a082c035c9
https://doi.org/10.1101/2022.10.22.22281386
https://doi.org/10.1101/2022.10.22.22281386
Autor:
Robert Loughnan, Jonathan Ahern, Cherisse Tompkins, Clare E. Palmer, John Iversen, Wesley K. Thompson, Ole Andreassen, Terry Jernigan, Leo Sugrue, Anders Dale, Mary E. T. Boyle, Chun Chieh Fan
Publikováno v:
JAMA neurology, vol 79, iss 9
ImportanceHereditary hemochromatosis (HH) is an autosomal recessive genetic disorder that leads to iron overload. Conflicting results from previous research has led some to believe the brain is spared the toxic effects of iron in HH.ObjectiveTo test
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4ba482097d374f429b397b057fac904
https://escholarship.org/uc/item/9gt7484s
https://escholarship.org/uc/item/9gt7484s
Autor:
Leo P. Sugrue, Chun Chieh Fan, Cherisse Thompkins, Terry L. Jernigan, Clare E. Palmer, Wesley Thompson, Mary Et Boyle, Ole A. Andreassen, Jonathan Ahern, John Iversen, Robert Loughnan, Anders M. Dale
Hereditary hemochromatosis (HH) is an autosomal recessive genetic disorder that can lead to iron overload, causing oxidative damage to affected organs. HH type 1 is predominantly associated with homozygosity for the mutation p.C282Y. Previous case st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::389052a38db349bf23a94f32ee06fe43
https://doi.org/10.1101/2021.08.16.21262117
https://doi.org/10.1101/2021.08.16.21262117