Citations for
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.
Guo Y, Tan LJ, Lei SF, Yang TL, Chen XD, Zhang F, Chen Y, Pan F, Yan H, Liu X, Tian Q, Zhang ZX, Zhou Q, Qiu C, Dong SS, Xu XH, Guo YF, Zhu XZ, Liu SL, Wang XL, Li X, Luo Y, Zhang LS, Li M, Wang JT, Wen T, Drees B, Hamilton J, Papasian CJ, Recker RR, Song XP, Cheng J, Deng HW.
PLoS Genet 6(1):e1000806.PMID: 20072603 2010
Biochemical and molecular characterization of 18 patients with pyridoxine-dependent epilepsy and mutations of the antiquitin (ALDH7A1) gene.
Plecko B, Paul K, Paschke E, Stoeckler-Ipsiroglu S, Struys E, Jakobs C, Hartmann H, Luecke T, di Capua M, Korenke C, Hikel C, Reutershahn E, Freilinger M, Baumeister F, Bosch F, Erwa W.
Hum Mutat 28(1):19-26. 2007
Allelic and non-allelic heterogeneities in pyridoxine dependent seizures revealed by ALDH7A1 mutational analysis.
Kanno J, Kure S, Narisawa A, Kamada F, Takayanagi M, Yamamoto K, Hoshino H, Goto T, Takahashi T, Haginoya K, Tsuchiya S, Baumeister FA, Hasegawa Y, Aoki Y, Yamaguchi S, Matsubara Y.
Mol Genet Metab 91(4):384-9. Epub 2007 Apr 11. 2007
Mutations in antiquitin in individuals with pyridoxine-dependent seizures.
Mills PB, Struys E, Jakobs C, Plecko B, Baxter P, Baumgartner M, Willemsen MA, Omran H, Tacke U, Uhlenberg B, Weschke B, Clayton PT.
Nat Med 12(3):307-9. Epub 2006 Feb 19. 2006
Antiquitin, a relatively unexplored member in the superfamily of aldehyde dehydrogenases with diversified physiological functions.
Fong WP, Cheng CH, Tang WK.
Cell Mol Life Sci 63(24):2881-5. Review. 2006
Human aldehyde dehydrogenase gene family.
Yoshida A, Rzhetsky A, Hsu LC, Chang C.
Eur J Biochem 251(3):549-57. 1998
An ancient conserved gene expressed in the human inner ear : identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1).
Skvorak AB, Robertson NG, Yin Y, Weremowicz S, Her H, Bieber FR, Beisel KW, Lynch ED, Beier DR, Morton CC.
Genomics 46(2):191-9. 1997