Clinical characterization of patients with idiopathic chronic pancreatitis and SPINK1 Mutations

A. Schneider Depts. of Medicine, Human Genetics, Cell Biology and Physiology, VA Pittsburgh Health Care System, and the Center for Genomic Sciences, University of Pittsburgh, Pittsburgh, PA, USA

M. M. Barmada Depts. of Medicine, Human Genetics, Cell Biology and Physiology, VA Pittsburgh Health Care System, and the Center for Genomic Sciences, University of Pittsburgh, Pittsburgh, PA, USA

A. Slivka Depts. of Medicine, Human Genetics, Cell Biology and Physiology, VA Pittsburgh Health Care System, and the Center for Genomic Sciences, University of Pittsburgh, Pittsburgh, PA, USA

J. A. Martin Depts. of Medicine, Human Genetics, Cell Biology and Physiology, VA Pittsburgh Health Care System, and the Center for Genomic Sciences, University of Pittsburgh, Pittsburgh, PA, USA

D. C. Whitcomb Depts. of Medicine, Human Genetics, Cell Biology and Physiology, VA Pittsburgh Health Care System, and the Center for Genomic Sciences, University of Pittsburgh, Pittsburgh, PA, USACorrespondence[email protected]

References

Etemad B, Whitcomb DC. Chronic pancreatitis: diagnosis, classification, and new genetic developments. Gastroenterology 2001;120:682–707.
PubMed Web of Science ®Google Scholar
Witt H, Luck W, Hennies HC, Classen M, Kage A, Lass U, et al. Mutations in the gene encoding the serine protease inhibitor, Kazal type 1 are associated with chronic pancreatitis. Nat Genet 2000;25:213–6.
PubMed Web of Science ®Google Scholar
Pfützer RH, Barmada MM, Brunskill AP, Finch R, Hart PS, Neoptolemos J, et al. SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis. Gastroenterology 2000;119: 615–23.
Google Scholar
Drenth JP, te Morsche R, Jansen JB. Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis. Gut 2002;50:687–92.
PubMed Web of Science ®Google Scholar
Threadgold J, Greenhalf W, Ellis I, Howes N, Lerch MM, Simon P, et al. The N34S mutation of SPINK1 (PSTI) is associated with a familial pattern of idiopathic chronic pancreatitis but does not cause the disease. Gut 2002;50:675–81.
PubMed Web of Science ®Google Scholar

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Clinical characterization of patients with idiopathic chronic pancreatitis and SPINK1 Mutations

References

Information for

Open access

Opportunities

Help and information

Your download is now in progress and you may close this window

Login or register to access this feature

Clinical characterization of patients with idiopathic chronic pancreatitis and SPINK1 Mutations

References

Reprints and Corporate Permissions

Academic Permissions

Related research

To cite this article:

Download citation

Information for

Open access

Opportunities

Help and information

Keep up to date