A novel mutation (c.855delG) in STK11 gene is associated with Peutz–Jeghers syndrome in a Chinese family. Issue 3 (March 2018)

Record Type:: Journal Article
Title:: A novel mutation (c.855delG) in STK11 gene is associated with Peutz–Jeghers syndrome in a Chinese family. Issue 3 (March 2018)
Main Title:: A novel mutation (c.855delG) in STK11 gene is associated with Peutz–Jeghers syndrome in a Chinese family
Authors:: Zhao, Zi-Ye
Jiang, Yu-Liang
Li, Bai-Rong
Yu, En-Da
Ning, Shou-Bin
Abstract:
Is Part Of:: Digestive and liver disease. Volume 50:Issue 3(2018)
Journal:: Digestive and liver disease
Issue:: Volume 50:Issue 3(2018)
Issue Display:: Volume 50, Issue 3 (2018)
Year:: 2018
Volume:: 50
Issue:: 3
Issue Sort Value:: 2018-0050-0003-0000
Page Start:: 312
Page End:: 314
Publication Date:: 2018-03
Subjects:: Digestive organs -- Diseases -- Periodicals
Liver -- Diseases -- Periodicals
616.33005
Journal URLs:: http://www.sciencedirect.com/science/journal/15908658 ↗
http://www.elsevier.com/journals ↗
DOI:: 10.1016/j.dld.2017.12.007 ↗
Languages:: English
ISSNs:: 1590-8658
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3588.345600
British Library DSC - BLDSS-3PM
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Ingest File:: 6193.xml