A revised allele frequency estimate and haplotype analysis of the DBH deficiency mutation IVS1+2T → C in African- and European-Americans

被引:12
作者
Zabetian, CP
Romero, R
Robertson, D
Sharma, S
Padbury, JF
Kuivaniemi, H
Kim, KS
Kim, CH
Köhnke, MD
Kranzler, HR
Gelernter, J
Cubells, JF
机构
[1] VA Puget Sound Hlth Care Syst, Dept Neurol, Seattle, WA 98108 USA
[2] Univ Washington, Sch Med, Dept Neurol, Seattle, WA USA
[3] Wayne State Univ, NICHHD, Perinatol Res Branch, Detroit, MI USA
[4] Vanderbilt Univ, Autonom Dysfunct Ctr, Dept Med, Nashville, TN USA
[5] Vanderbilt Univ, Autonom Dysfunct Ctr, Dept Pharmacol, Nashville, TN USA
[6] Vanderbilt Univ, Autonom Dysfunct Ctr, Dept Neurol, Nashville, TN USA
[7] Brown Univ, Sch Med, Dept Pediat, Providence, RI 02912 USA
[8] Womens & Childrens Hosp, Providence, RI USA
[9] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI USA
[10] Harvard Univ, McLean Hosp, Sch Med, Mol Neurobiol Lab, Belmont, MA 02178 USA
[11] Tuebingen Univ Hosp, Univ Hosp Psychiat & Psychotherapy, Tubingen, Germany
[12] Univ Connecticut, Sch Med, Alcohol Res Ctr, Dept Psychiat, Farmington, CT USA
[13] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA
[14] VA Connecticut Healthcare Syst, Dept Psychiat, West Haven, CT USA
关键词
D O I
10.1002/ajmg.a.20300
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:190 / 192
页数:3
相关论文
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