Gene of the issue – RUNX1 mutations and inherited bleeding

Neil Morgan; Martina E Daly

doi:10.1080/09537104.2017.1280151

Gene of the issue – RUNX1 mutations and inherited bleeding

Neil Morgan, Martina E Daly

Cardiovascular Sciences

Research output: Contribution to journal › Review article › peer-review

7 Citations (Scopus)

198 Downloads (Pure)

Original language	English
Pages (from-to)	208-210
Journal	Platelets
Volume	28
Issue number	2
Early online date	17 Feb 2017
DOIs	https://doi.org/10.1080/09537104.2017.1280151
Publication status	Published - 2017

Keywords

platelets
bleeding
RUNX1 mutations
genetics

Access to Document

10.1080/09537104.2017.1280151Licence: Creative Commons: Attribution (CC BY)

Morgan_Daly_Gene_of_the_issue_PlateletsFinal published version, 560 KBLicence: Creative Commons: Attribution (CC BY)

Identification and functional investigation of genes in patients with inherited bleeding disorders
Morgan, N. & Watson, S.
British Heart Foundation
28/09/15 → 27/09/18
Project: Research
Molecular Genetic Investigation of Patients with Congenital Thrombocytopenias
Morgan, N., Harrison, P., Lowe, G. & Watson, S.
British Heart Foundation
18/11/13 → 17/11/16
Project: Research

Cite this

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title = "Gene of the issue – RUNX1 mutations and inherited bleeding",

keywords = "platelets, bleeding, RUNX1 mutations, genetics",

author = "Neil Morgan and Daly, {Martina E}",

year = "2017",

doi = "10.1080/09537104.2017.1280151",

language = "English",

volume = "28",

pages = "208--210",

journal = "Platelets",

issn = "0953-7104",

publisher = "Taylor & Francis",

number = "2",

}

TY - JOUR

T1 - Gene of the issue – RUNX1 mutations and inherited bleeding

AU - Morgan, Neil

AU - Daly, Martina E

PY - 2017

Y1 - 2017

KW - platelets

KW - bleeding

KW - RUNX1 mutations

KW - genetics

U2 - 10.1080/09537104.2017.1280151

DO - 10.1080/09537104.2017.1280151

M3 - Review article

C2 - 28277065

SN - 0953-7104

VL - 28

SP - 208

EP - 210

JO - Platelets

JF - Platelets

IS - 2

ER -

Gene of the issue – RUNX1 mutations and inherited bleeding

Keywords

Access to Document

Projects

Identification and functional investigation of genes in patients with inherited bleeding disorders

Molecular Genetic Investigation of Patients with Congenital Thrombocytopenias

Cite this