A serine/threonine kinase gene defective in Peutz–Jeghers syndrome
A serine/threonine kinase gene defective in Peutz–Jeghers syndrome
About this item
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Author / Creator
Hemminki, Akseli , Markie, David , Tomlinson, Ian , Avizienyte, Egle , Roth, Stina , Loukola, Anu , Bignell, Graham , Warren, William , Aminoff, Maria , Höglund, Pia , Järvinen, Heikki , Kristo, Paula , Pelin, Katarina , Ridanpää, Maaret , Salovaara, Reijo , Toro, Tumi , Bodmer, Walter , Olschwang, Sylviane , Olsen, Anne S. , Stratton, Michael R. , de la Chapelle, Albert and Aaltonen, Lauri A.
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
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More information
Scope and Contents
Contents
Studies of hereditary cancer syndromes have contributed greatly to our understanding of molecular events involved in tumorigenesis. Here we investigate the molecular background of the Peutz–Jeghers syndrome
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,
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(PJS), a rare hereditary disease in which there is predisposition to benign and malignant tumours of many organ systems. A lo...
Alternative Titles
Full title
A serine/threonine kinase gene defective in Peutz–Jeghers syndrome
Authors, Artists and Contributors
Author / Creator
Markie, David
Tomlinson, Ian
Avizienyte, Egle
Roth, Stina
Loukola, Anu
Bignell, Graham
Warren, William
Aminoff, Maria
Höglund, Pia
Järvinen, Heikki
Kristo, Paula
Pelin, Katarina
Ridanpää, Maaret
Salovaara, Reijo
Toro, Tumi
Bodmer, Walter
Olschwang, Sylviane
Olsen, Anne S.
Stratton, Michael R.
de la Chapelle, Albert
Aaltonen, Lauri A.
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_79660909
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_79660909
Other Identifiers
ISSN
0028-0836
E-ISSN
1476-4687
DOI
10.1038/34432
