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Genetic heterogeneity in Peutz-Jeghers syndrome

Genetic heterogeneity in Peutz-Jeghers syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_71224645

Genetic heterogeneity in Peutz-Jeghers syndrome

About this item

Full title

Genetic heterogeneity in Peutz-Jeghers syndrome

Publisher

New York: John Wiley & Sons, Inc

Journal title

Human mutation, 2000-07, Vol.16 (1), p.23-30

Language

English

Formats

Publication information

Publisher

New York: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

LKB1, the human gene encoding a serine threonine kinase, was recently identified as a susceptibility gene for Peutz‐Jeghers syndrome (PJS), a disease characterized by the constellation of intestinal hamartomata, oral mucocutaneous hyperpigmentation, and an increased risk for gastrointestinal as well as extraintestinal malignancies. To date, the maj...

Alternative Titles

Full title

Genetic heterogeneity in Peutz-Jeghers syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_71224645

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_71224645

Other Identifiers

ISSN

1059-7794

E-ISSN

1098-1004

DOI

10.1002/1098-1004(200007)16:1<23::AID-HUMU5>3.0.CO;2-M

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