UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

EXOME SEQUENCING IDENTIFIES A HYPERMORPHIC MISSENSE MUTATION IN THE PLCG2 GENE AS THE CAUSE OF A DOMINANTLY INHERITED AUTOINFLAMMATORY DISEASE WITH IMMUNODEFICIENCY

Aksentijevich, I; Zhou, Q; Lee, G-S; Katan, M; Datta, S; Milner, J; Khan, J; (2013) EXOME SEQUENCING IDENTIFIES A HYPERMORPHIC MISSENSE MUTATION IN THE PLCG2 GENE AS THE CAUSE OF A DOMINANTLY INHERITED AUTOINFLAMMATORY DISEASE WITH IMMUNODEFICIENCY. ANNALS OF THE RHEUMATIC DISEASES , 71 pp. 113-114. 10.1136/annrheumdis-2012-eular.1857.

Full text not available from this repository.
Type: Article
Title: EXOME SEQUENCING IDENTIFIES A HYPERMORPHIC MISSENSE MUTATION IN THE PLCG2 GENE AS THE CAUSE OF A DOMINANTLY INHERITED AUTOINFLAMMATORY DISEASE WITH IMMUNODEFICIENCY
DOI: 10.1136/annrheumdis-2012-eular.1857
Keywords: Science & Technology, Life Sciences & Biomedicine, Rheumatology
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > Div of Biosciences > Structural and Molecular Biology
URI: http://discovery.ucl.ac.uk/id/eprint/1430444
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item