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Details on Person Thromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)

Class:IdLiteratureReference:5618151
_displayNameThromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)
_timestamp2014-08-19 12:54:50
author[Person:5618162] Geneviève, David
[Person:5618140] Proulle, Valérie
[Person:3322924] Isidor, Bertrand
[Person:5618153] Bellais, Samuel
[Person:5618152] Serre, Valérie
[Person:5618142] Djouadi, Fatima
[Person:1679061] Picard, C
[Person:5618144] Vignon-Savoye, Capucine
[Person:4722110] Bader-Meunier, Brigitte
[Person:5618139] Blanche, Stéphane
[Person:5618146] de Vernejoul, Marie-Christine
[Person:2045015] Legeai-Mallet, L
[Person:5618148] Fischer, Anne-Marie
[Person:2029770] Le Merrer, M
[Person:5618157] Dreyfus, Marie
[Person:5618150] Gaussem, Pascale
[Person:2038337] Munnich, A
[Person:2426338] Cormier-Daire, Valerie
created[InstanceEdit:5618145] Jassal, Bijay, 2014-08-19
journalNat. Genet.
pages284-6
pubMedIdentifier18264100
titleThromboxane synthase mutations in an increased bone density disorder (Ghosal syndrome)
volume40
year2008
(literatureReference)[Pathway:5579032] Defective TBXAS1 causes GHDD [Homo sapiens]
[FailedReaction:5603275] Defective TBXAS1 does not isomerise PGH2 to TXA2 [Homo sapiens]
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