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1987 2
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Page 1
Biochemistry and genetics of monoamine oxidase.
Weyler W, Hsu YP, Breakefield XO. Weyler W, et al. Pharmacol Ther. 1990;47(3):391-417. doi: 10.1016/0163-7258(90)90064-9. Pharmacol Ther. 1990. PMID: 2290855 Review.
Mutations in the Norrie disease gene.
Schuback DE, Chen ZY, Craig IW, Breakefield XO, Sims KB. Schuback DE, et al. Hum Mutat. 1995;5(4):285-92. doi: 10.1002/humu.1380050403. Hum Mutat. 1995. PMID: 7627181
Mutational analysis of the human MAOA gene.
Tivol EA, Shalish C, Schuback DE, Hsu YP, Breakefield XO. Tivol EA, et al. Am J Med Genet. 1996 Feb 16;67(1):92-7. doi: 10.1002/(SICI)1096-8628(19960216)67:1<92::AID-AJMG16>3.0.CO;2-K. Am J Med Genet. 1996. PMID: 8678123
Structure of the human gene for monoamine oxidase type A.
Chen ZY, Hotamisligil GS, Huang JK, Wen L, Ezzeddine D, Aydin-Muderrisoglu N, Powell JF, Huang RH, Breakefield XO, Craig I, et al. Chen ZY, et al. Nucleic Acids Res. 1991 Aug 25;19(16):4537-41. doi: 10.1093/nar/19.16.4537. Nucleic Acids Res. 1991. PMID: 1886775 Free PMC article.
Screen for MAOA mutations in target human groups.
Schuback DE, Mulligan EL, Sims KB, Tivol EA, Greenberg BD, Chang SF, Yang SL, Mau YC, Shen CY, Ho MS, Yang NH, Butler MG, Fink S, Schwartz CE, Berlin F, Breakefield XO, Murphy DL, Hsu YP. Schuback DE, et al. Am J Med Genet. 1999 Feb 5;88(1):25-8. Am J Med Genet. 1999. PMID: 10050962 Free PMC article.
24 results