PLA2G6, encoding a phospholipase A 2, is mutated in neurodegenerative disorders with high brain iron

Nature Genetics

Volumn 38, Issue 7, 2006, Pages 752-754

  Morgan, Neil V ^a   Westaway, Shawn K ^b   Morton, Jenny E V ^c   Gregory, Allison ^b   Gissen, Paul ^a   Sonek, Scott ^b   Cangul, Hakan ^a,d   Coryell, Jason ^b   Canham, Natalie ^c   Nardocci, Nardo ^e   Zorzi, Giovanna ^e   Pasha, Shanaz ^a   Rodriguez, Diana ^f   Desguerre, Isabelle ^g   Mubaidin, Amar ^h   Bertini, Enrico ⁱ   Trembath, Richard C ^j   Simonati, Alessandro ^k   Schanen, Carolyn ^l   Johnson, Colin A ^a   Levinson, Barbara ^m   Woods, C Geoffrey ⁿ   Wilmot, Beth ^b   Kramer, Patricia ^b,o   Gitschier, Jane ^m,p   Maher, Eamonn R ^a,c   Hayflick, Susan J ^b,o,q   more..

^a UNIVERSITY DEPARTMENT OF MEDICINE   (United Kingdom)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^c BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^d ULUDAG UNIVERSITY   (Turkey)

^e DEPARTMENT OF NEUROSURGERY   (Italy)

^f ARMAND TROUSSEAU HOSPITAL   (France)

^g HÔPITAL NECKER ENFANTS MALADES   (France)

^h KING HUSSEIN MEDICAL CENTER   (Jordan)

ⁱ BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^j GUY S HOSPITAL   (United Kingdom)

^k UNIVERSITY OF VERONA   (Italy)

^l NEMOURS ALFRED I DUPONT HOSPITAL FOR CHILDREN   (United States)

^m UNIVERSITY OF CALIFORNIA   (United States)

ⁿ UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^o OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^p HOWARD HUGHES MEDICAL INSTITUTE   (United States)

^q OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM; IRON; PHOSPHOLIPASE A2;

ALZHEIMER DISEASE; ARTICLE; CHROMOSOME 22Q; DEGENERATIVE DISEASE; FRAMESHIFT MUTATION; GENE; GENE LOCUS; GENE MAPPING; GENE MUTATION; HOMEOSTASIS; HUMAN; KARAK SYNDROME; MISSENSE MUTATION; NERVE DEGENERATION; NEUROAXONAL DYSTROPHY; PARKINSON DISEASE; PATHOGENESIS; PLA2G6 GENE; PRIORITY JOURNAL;

BRAIN; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HEREDODEGENERATIVE DISORDERS, NERVOUS SYSTEM; HUMANS; IRON; MALE; MUTATION; NEUROAXONAL DYSTROPHIES; PHOSPHOLIPASES A; SYNDROME;

EID: 33745553895     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1826     Document Type: Article

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