Targeted Exome Sequencing of Genes Involved in Rare CNVs in Early-Onset Severe Obesity.

Loid, Petra; Pekkinen, Minna; Mustila, Taina; Tossavainen, Päivi; Viljakainen, Heli; Lindstrand, Anna; Mäkitie, Outi

Loid, Petra; Pekkinen, Minna; Mustila, Taina; Tossavainen, Päivi; Viljakainen, Heli; Lindstrand, Anna; Mäkitie, Outi.

Afiliação

Loid P; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Pekkinen M; Folkhälsan Research Center, Genetics Research Program, Helsinki, Finland.
Mustila T; Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Tossavainen P; Children's Hospital, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Viljakainen H; Folkhälsan Research Center, Genetics Research Program, Helsinki, Finland.
Lindstrand A; Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Mäkitie O; City of Turku Wellfare Services, Diabetes Care, Turku, Finland.

Front Genet ; 13: 839349, 2022.

Article em En | MEDLINE | ID: mdl-35330733

Palavras-chave

candidate genes; childhood obesity; copy number variants; gene panel; rare variants

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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Finlândia

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