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Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation

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Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation. / Kakar, Naseebullah; Ahmad, Jamil; Kubisch, Christian; Borck, Guntram.

in: AM J MED GENET A, Jahrgang 161, Nr. 10, 01.10.2013, S. 2672-4.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › Andere (Vorworte u.ä.) › Forschung

Harvard

Kakar, N, Ahmad, J, Kubisch, C & Borck, G 2013, 'Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation', AM J MED GENET A, Jg. 161, Nr. 10, S. 2672-4. https://doi.org/10.1002/ajmg.a.36125

APA

Kakar, N., Ahmad, J., Kubisch, C., & Borck, G. (2013). Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation. AM J MED GENET A, 161(10), 2672-4. https://doi.org/10.1002/ajmg.a.36125

Vancouver

Kakar N, Ahmad J, Kubisch C, Borck G. Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation. AM J MED GENET A. 2013 Okt 1;161(10):2672-4. https://doi.org/10.1002/ajmg.a.36125

Bibtex

@article{4b7d613875404b1590827c2513a4bc77,
title = "Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation",
keywords = "Age of Onset, Alternative Splicing, Child, Child, Preschool, Consanguinity, DNA Mutational Analysis, Exons, Female, Humans, Male, Mutation, Obesity, RNA Splice Sites, Receptors, Leptin",
author = "Naseebullah Kakar and Jamil Ahmad and Christian Kubisch and Guntram Borck",
note = "Letter",
year = "2013",
month = oct,
day = "1",
doi = "10.1002/ajmg.a.36125",
language = "English",
volume = "161",
pages = "2672--4",
journal = "AM J MED GENET A",
issn = "1552-4825",
publisher = "Wiley-Liss Inc.",
number = "10",

}

RIS

TY - JOUR

T1 - Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation

AU - Kakar, Naseebullah

AU - Ahmad, Jamil

AU - Kubisch, Christian

AU - Borck, Guntram

N1 - Letter

PY - 2013/10/1

Y1 - 2013/10/1

KW - Age of Onset

KW - Alternative Splicing

KW - Child

KW - Child, Preschool

KW - Consanguinity

KW - DNA Mutational Analysis

KW - Exons

KW - Female

KW - Humans

KW - Male

KW - Mutation

KW - Obesity

KW - RNA Splice Sites

KW - Receptors, Leptin

U2 - 10.1002/ajmg.a.36125

DO - 10.1002/ajmg.a.36125

M3 - Other (editorial matter etc.)

C2 - 23949901

VL - 161

SP - 2672

EP - 2674

JO - AM J MED GENET A

JF - AM J MED GENET A

SN - 1552-4825

IS - 10

ER -