LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity
LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity
About this item
Full title
Author / Creator
Tajan, Mylène , Batut, Aurélie , Cadoudal, Thomas , Deleruyelle, Simon , Le Gonidec, Sophie , Saint Laurent, Céline , Vomscheid, Maëlle , Wanecq, Estelle , Tréguer, Karine , De Rocca Serra-Nédélec, Audrey , Vinel, Claire , Marques, Marie-Adeline , Pozzo, Joffrey , Kunduzova, Oksana , Salles, Jean-Pierre , Tauber, Maithé , Raynal, Patrick , Cavé, Hélène , Edouard, Thomas , Valet, Philippe and Yart, Armelle
Publisher
United States: National Academy of Sciences
Journal title
Language
English
Formats
Publication information
Publisher
United States: National Academy of Sciences
Subjects
More information
Scope and Contents
Contents
Significance LEOPARD syndrome (multiple L entigines, E lectrocardiographic conduction abnormalities, O cular hypertelorism, P ulmonary stenosis, A bnormal genitalia, R etardation of growth, sensorineural D eafness; LS) is a rare genetic disease associating various developmental defects mainly caused by inactivating mutations of the tyrosine phospha...
Alternative Titles
Full title
LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity
Authors, Artists and Contributors
Author / Creator
Batut, Aurélie
Cadoudal, Thomas
Deleruyelle, Simon
Le Gonidec, Sophie
Saint Laurent, Céline
Vomscheid, Maëlle
Wanecq, Estelle
Tréguer, Karine
De Rocca Serra-Nédélec, Audrey
Vinel, Claire
Marques, Marie-Adeline
Pozzo, Joffrey
Kunduzova, Oksana
Salles, Jean-Pierre
Tauber, Maithé
Raynal, Patrick
Cavé, Hélène
Edouard, Thomas
Valet, Philippe
Yart, Armelle
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_1615739007
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_1615739007
Other Identifiers
ISSN
0027-8424,1091-6490
E-ISSN
1091-6490
DOI
10.1073/pnas.1406107111
