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Başlık: PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron
Yazarlar: Morgan, Neil V.
Westaway, Shawn K
Morton, Jenny E. V.
Gregory, Allison
Gissen, Paul
Sonek, Scott
Coryell, Jason
Canham, Natalie
Nardocci, Nardo
Giovanna, Giovanna
Shanaz, Shanaz
Rodriguez, Diana
Desguerre, Isabelle
Mubaidin, Amar
Bertin, Enrico
Trembath, Richard C.
Simonati, Alessandro
Schanen, Carolyn
Johnson, Colin A.
Levinson, Barbara
Woods, C. Geoffrey
Wilmot, Beth
Kramer, Patricia
Gitschier, Jane
Maher, Eamonn R.
Hayflick, Susan J.
Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı.
Cangül, Hakan
8911611600
Anahtar kelimeler: Genetics & heredity
Involvement
Hallervorden-spatz-syndrome
Infantile neuroaxonal dystrophy
Yayın Tarihi: 2006
Yayıncı: Nature Publishing Group
Atıf: Morgan, N. V. vd. (2006). ''PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron''. Nature Genetics, 38(7), 752-754.
Özet: Neurodegenerative disorders with high brain iron include Parkinson disease, Alzheimer disease and several childhood genetic disorders categorized as neuroaxonal dystrophies. We mapped a locus for infantile neuroaxonal dystrophy ( INAD) and neurodegeneration with brain iron accumulation (NBIA) to chromosome 22q12-q13 and identified mutations in PLA2G6, encoding a calcium-independent group VI phospholipase A(2), in NBIA, INAD and the related Karak syndrome. This discovery implicates phospholipases in the pathogenesis of neurodegenerative disorders with iron dyshomeostasis.
URI: https://doi.org/10.1038/ng1826
1061-4036
http://hdl.handle.net/11452/21406
ISSN: 1061-4036
Koleksiyonlarda Görünür:Scopus
Web of Science

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