A Form of the Metabolic Syndrome Associated with Mutations inDYRK1B
Author(s) -
Ali R. Keramati,
Mohsen Fathzadeh,
Gwangwoong Go,
Rajvir Singh,
Murim Choi,
Saeed Faramarzi,
Shrikant Mane,
Mohammad Mehdi Kasaei,
Kazem Sarajzadeh-Fard,
John Hwa,
Kenneth K. Kídd,
Mohammad Ali Babaee Bigi,
Reza Malekzadeh,
A Hosseinian,
Masoud Babaei,
Richard P. Lifton,
Arya Mani
Publication year - 2014
Publication title -
new england journal of medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 19.889
H-Index - 1030
eISSN - 1533-4406
pISSN - 0028-4793
DOI - 10.1056/nejmoa1301824
Subject(s) - metabolic syndrome , genetics , mutation , gene , bioinformatics , medicine , biology , obesity
Genetic analysis has been successful in identifying causative mutations for individual cardiovascular risk factors. Success has been more limited in mapping susceptibility genes for clusters of cardiovascular risk traits, such as those in the metabolic syndrome.
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