Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502)))

J. Eisenberg; G. Mei-Tal; A. Steinberg; E. Tartakovsky; A. Zohar; I. Gritsenko; L. Nemanov; R. P. Ebstein

Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502)))

J. Eisenberg, G. Mei-Tal, A. Steinberg, E. Tartakovsky, A. Zohar, I. Gritsenko, L. Nemanov, R. P. Ebstein

Department of General History

Research output: Contribution to journal › Comment/debate

Original language	English
Pages (from-to)	893
Number of pages	1
Journal	American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
Volume	96
Issue number	6
State	Published - 4 Dec 2000

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Cite this

Eisenberg, J., Mei-Tal, G., Steinberg, A., Tartakovsky, E., Zohar, A., Gritsenko, I., Nemanov, L., & Ebstein, R. P. (2000). Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502))). American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 96(6), 893.

Eisenberg, J. ; Mei-Tal, G. ; Steinberg, A. et al. / Erratum : Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502))). In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 2000 ; Vol. 96, No. 6. pp. 893.

@article{ca08d279eabd4d31af9d74011214c994,

title = "Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502)))",

author = "J. Eisenberg and G. Mei-Tal and A. Steinberg and E. Tartakovsky and A. Zohar and I. Gritsenko and L. Nemanov and Ebstein, {R. P.}",

year = "2000",

month = dec,

day = "4",

language = "אנגלית",

volume = "96",

pages = "893",

journal = "American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics",

issn = "1552-4841",

publisher = "Wiley-Liss Inc.",

number = "6",

}

Eisenberg, J, Mei-Tal, G, Steinberg, A, Tartakovsky, E, Zohar, A, Gritsenko, I, Nemanov, L & Ebstein, RP 2000, 'Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502)))', American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, vol. 96, no. 6, pp. 893.

Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502))). / Eisenberg, J.; Mei-Tal, G.; Steinberg, A. et al.
In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 96, No. 6, 04.12.2000, p. 893.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Erratum

T2 - Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502)))

AU - Eisenberg, J.

AU - Mei-Tal, G.

AU - Steinberg, A.

AU - Tartakovsky, E.

AU - Zohar, A.

AU - Gritsenko, I.

AU - Nemanov, L.

AU - Ebstein, R. P.

PY - 2000/12/4

Y1 - 2000/12/4

UR - http://www.scopus.com/inward/record.url?scp=0034606208&partnerID=8YFLogxK

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.comment???

AN - SCOPUS:0034606208

SN - 1552-4841

VL - 96

SP - 893

JO - American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

JF - American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

IS - 6

ER -

Eisenberg J, Mei-Tal G, Steinberg A, Tartakovsky E, Zohar A, Gritsenko I et al. Erratum: Haplotype relative risk study of catechol-o-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity Val allele with ADHD impulsive-hyperactive phenotype (American Journal of Medical Genetics (Neuropsychiatic Genetics 88:5 (497-502))). American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 2000 Dec 4;96(6):893.

UN SDGs

Other files and links

Cite this