CFTR gene mutations in pancreatitis: Frequency and clinical manifestations in an Austrian patient cohort (Q57637000)

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9 January 2020

title

CFTR gene mutations in pancreatitis: Frequency and clinical manifestations in an Austrian patient cohort (English)

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9 January 2020

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5

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9 January 2020

author name string

Heinz Zoller

1

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9 January 2020

Margit Egg

2

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9 January 2020

Ivo Graziadei

3

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9 January 2020

Marc Creus

4

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9 January 2020

Judith Löffler-Ragg

6

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9 January 2020

Wolfgang Vogel

7

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9 January 2020

publication date

1 January 2007

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9 January 2020

published in

Vienna Clinical Weekly

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9 January 2020

volume

119

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issue

17-18

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9 January 2020

page(s)

527-533

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https://scigraph.springernature.com/pub.10.1007/s00508-007-0849-5

9 January 2020

exact match

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cites work

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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene

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Calcium-pump inhibitors induce functional surface expression of Delta F508-CFTR protein in cystic fibrosis epithelial cells

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Absence of association between SPINK1 trypsin inhibitor mutations and Type 1 or 2 diabetes mellitus in India and Germany

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Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls

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Risk of pancreatitis with mutation of the cystic fibrosis gene

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12 December 2020

Different CFTR mutational spectrum in alcoholic and idiopathic chronic pancreatitis?

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12 December 2020

Chronic pancreatitis: etiology, pathogenesis, diagnosis, and treatment

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SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis

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Mutations of the cystic fibrosis gene in patients with chronic pancreatitis

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12 December 2020

Chronic pancreatitis: diagnosis, classification, and new genetic developments

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12 December 2020

10.1007/S00508-007-0849-5

Identifiers

DOI

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9 January 2020

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