Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

Trine W Boesgaard; Stepanka Pruhova; Ehm Astrid Andersson; Ondrej Cinek; Barbora Obermannova; Jeannet Lauenborg; Peter Damm; Regine Bergholdt; Flemming  Pociot; Charlotta Pisinger; Fabrizio Barbetti; Jan Lebl; Oluf Pedersen; Torben Hansen

doi:10.1186/1471-2350-11-42

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

Trine W Boesgaard, Stepanka Pruhova, Ehm Astrid Andersson, Ondrej Cinek, Barbora Obermannova, Jeannet Lauenborg, Peter Damm, Regine Bergholdt, Flemming Pociot, Charlotta Pisinger, Fabrizio Barbetti, Jan Lebl, Oluf Pedersen, Torben Hansen

70 Citations (Scopus)

Abstract

Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.

Original language	English
Journal	B M C Medical Genetics
Volume	11
Pages (from-to)	42
ISSN	1471-2350
DOIs	https://doi.org/10.1186/1471-2350-11-42
Publication status	Published - 1 Jan 2010

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Boesgaard, T. W., Pruhova, S., Andersson, E. A., Cinek, O., Obermannova, B., Lauenborg, J., Damm, P., Bergholdt, R., Pociot, F., Pisinger, C., Barbetti, F., Lebl, J., Pedersen, O., & Hansen, T. (2010). Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). B M C Medical Genetics, 11, 42. https://doi.org/10.1186/1471-2350-11-42

Boesgaard, TW, Pruhova, S, Andersson, EA, Cinek, O, Obermannova, B, Lauenborg, J , Damm, P, Bergholdt, R, Pociot, F , Pisinger, C, Barbetti, F, Lebl, J, Pedersen, O & Hansen, T 2010, 'Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)', B M C Medical Genetics, vol. 11, pp. 42. https://doi.org/10.1186/1471-2350-11-42

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abstract = "Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.",

author = "Boesgaard, {Trine W} and Stepanka Pruhova and Andersson, {Ehm Astrid} and Ondrej Cinek and Barbora Obermannova and Jeannet Lauenborg and Peter Damm and Regine Bergholdt and Flemming Pociot and Charlotta Pisinger and Fabrizio Barbetti and Jan Lebl and Oluf Pedersen and Torben Hansen",

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AU - Boesgaard, Trine W

AU - Pruhova, Stepanka

AU - Andersson, Ehm Astrid

AU - Cinek, Ondrej

AU - Obermannova, Barbora

AU - Lauenborg, Jeannet

AU - Damm, Peter

AU - Bergholdt, Regine

AU - Pociot, Flemming

AU - Pisinger, Charlotta

AU - Barbetti, Fabrizio

AU - Lebl, Jan

AU - Pedersen, Oluf

AU - Hansen, Torben

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N2 - Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.

AB - Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.

U2 - 10.1186/1471-2350-11-42

DO - 10.1186/1471-2350-11-42

M3 - Journal article

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VL - 11

SP - 42

JO - B M C Medical Genetics

JF - B M C Medical Genetics

ER -

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

Abstract

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