Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family.

Bonnefond, A; Vaillant, E; Philippe, J; Skrobek, B; Lobbens, S; Yengo, L; Huyvaert, M; Cavé, H; Busiah, K; Scharfmann, R; Polak, M; Abdul-Rasoul, M; Froguel, P; Vaxillaire, M

Bonnefond, A; Vaillant, E; Philippe, J; Skrobek, B; Lobbens, S; Yengo, L; Huyvaert, M; Cavé, H; Busiah, K; Scharfmann, R; Polak, M; Abdul-Rasoul, M; Froguel, P; Vaxillaire, M.

Affiliation

Bonnefond A; European Genomic Institute for Diabetes (EGID) FR 3508, 59000 Lille, France.

Diabetes Metab ; 39(3): 276-80, 2013 May.

Article in En | MEDLINE | ID: mdl-23562494

Subject(s)

Consanguinity; Diabetes Mellitus/genetics; Homeodomain Proteins/genetics; Infant, Newborn, Diseases/genetics; Transcription Factors/genetics; Diabetes Mellitus/diagnosis; Female; Humans; Infant, Newborn; Infant, Newborn, Diseases/diagnosis; Sequence Analysis, DNA

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / Homeodomain Proteins / Consanguinity / Diabetes Mellitus / Infant, Newborn, Diseases Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Newborn Language: En Journal: Diabetes Metab Year: 2013 Document type: Article

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