Mutation in GNE is associated with severe congenital thrombocytopenia-Reference-Cited by-同舟云学术

Mutation in GNE is associated with severe congenital thrombocytopenia

Published:2018-10-25 Issue:17 Volume:132 Page:1855-1858
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Futterer Jane¹,Dalby Amanda¹,Lowe Gillian C.¹,Johnson Ben¹,Simpson Michael A.²,Motwani Jayashree³,Williams Mike³,Watson Steve P.¹,Morgan Neil V.¹^ORCID

Affiliation:

1. Institute of Cardiovascular Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom;

2. Division of Genetics and Molecular Medicine, King’s College, London, United Kingdom; and

3. Department of Haematology, Birmingham Children’s Hospital, Birmingham, United Kingdom

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/132/17/1855/1467959/blood847798.pdf

Reference16 articles.

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2. Exomic sequencing identifies PALB2 as a pancreatic cancer susceptibility gene;Jones;Science,2009

3. Recurring mutations found by sequencing an acute myeloid leukemia genome;Mardis;N Engl J Med,2009

4. Targeted capture and massively parallel sequencing of 12 human exomes;Ng;Nature,2009

5. Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects;Johnson;Haematologica,2016

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