(Q28344965)

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Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis

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Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis (English)

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2

E Myers

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John P Neoptolemos

object named as

J Neoptolemos

series ordinal

6

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author name string

R Pfützer

series ordinal

1

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S Applebaum-Shapiro

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3

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R Finch

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4

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I Ellis

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5

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J A Kant

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7

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D C Whitcomb

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8

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language of work or name

English

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publication date

February 2002

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published in

Gut

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volume

50

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issue

2

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page(s)

271-2

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cites work

Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773118

retrieved

20 March 2017

Hereditary pancreatitis and the risk of pancreatic cancer. International Hereditary Pancreatitis Study Group

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773118

retrieved

20 March 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773118

retrieved

20 March 2017

Human cationic trypsinogen. Role of Asn-21 in zymogen activation and implications in hereditary pancreatitis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773118

retrieved

2 June 2018

Genetic testing. Counseling, laboratory, and regulatory issues and the EUROPAC protocol for ethical research in multicenter studies of inherited pancreatic diseases.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1773118

retrieved

27 November 2018

Hereditary pancreatitis

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11788572

retrieved

12 December 2020

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ResearchGate publication ID

273879181

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(Q28344965)

Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis

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