A resequencing program in India detects the rare JAK2 L579F mutation in patients suffering from polycythemia vera and negative for JAK2 V617F. (6th September 2013)

Record Type:: Journal Article
Title:: A resequencing program in India detects the rare JAK2 L579F mutation in patients suffering from polycythemia vera and negative for JAK2 V617F. (6th September 2013)
Main Title:: A resequencing program in India detects the rare JAK2 L579F mutation in patients suffering from polycythemia vera and negative for JAK2 V617F
Authors:: Acharya, A.
Vaniawala, S.
Parekh, H.
Sheikh, H.
Patel, H.
Ali, R.
Khan, A.
Nagee, A.
Kunjadia, P.
Mukhopadhyaya, P. N.
Abstract:
Is Part Of:: International journal of laboratory hematology. Volume 36:Number 4(2014:Aug.)
Journal:: International journal of laboratory hematology
Issue:: Volume 36:Number 4(2014:Aug.)
Issue Display:: Volume 36, Issue 4 (2014)
Year:: 2014
Volume:: 36
Issue:: 4
Issue Sort Value:: 2014-0036-0004-0000
Page Start:: e30
Page End:: e33
Publication Date:: 2013-09-06
Subjects:: Hematology -- Periodicals
Blood -- Diseases -- Periodicals
Hematology -- Periodicals
616.15005
Journal URLs:: http://firstsearch.oclc.org/FSIP?db=ECO&journal=1751-5521&screen=info&done=referer ↗
http://www.blackwell-synergy.com/loi/clh ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1751-553X ↗
http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/ijlh.12141 ↗
Languages:: English
ISSNs:: 1751-5521
Deposit Type:: Legaldeposit
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Ingest File:: 3658.xml