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

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Standard

Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). / Boesgaard, Trine W; Pruhova, Stepanka; Andersson, Ehm A; Cinek, Ondrej; Obermannova, Barbora; Lauenborg, Jeannet; Damm, Peter; Bergholdt, Regine; Pociot, Flemming; Pisinger, Charlotta; Barbetti, Fabrizio; Lebl, Jan; Pedersen, Oluf; Hansen, Torben.

In: B M C Medical Genetics, Vol. 11, 01.01.2010, p. 42.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

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

APA

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

Vancouver

Boesgaard TW, Pruhova S, Andersson EA, Cinek O, Obermannova B, Lauenborg J et al. Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). B M C Medical Genetics. 2010 Jan 1;11:42. https://doi.org/10.1186/1471-2350-11-42

Author

Boesgaard, Trine W ; Pruhova, Stepanka ; Andersson, Ehm A ; Cinek, Ondrej ; Obermannova, Barbora ; Lauenborg, Jeannet ; Damm, Peter ; Bergholdt, Regine ; Pociot, Flemming ; Pisinger, Charlotta ; Barbetti, Fabrizio ; Lebl, Jan ; Pedersen, Oluf ; Hansen, Torben. / Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). In: B M C Medical Genetics. 2010 ; Vol. 11. pp. 42.

Bibtex

@article{5a4f0ce907ef405fa8f09101fd28372a,
title = "Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)",
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.",
keywords = "Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Diabetes, Gestational, Female, Genetic Variation, Humans, Insulin, Male, Mutation, Pedigree, Phenotype, Pregnancy, Young Adult",
author = "Boesgaard, {Trine W} and Stepanka Pruhova and Andersson, {Ehm A} 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",
year = "2010",
month = jan,
day = "1",
doi = "10.1186/1471-2350-11-42",
language = "English",
volume = "11",
pages = "42",
journal = "B M C Medical Genetics",
issn = "1471-2350",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

AU - Boesgaard, Trine W

AU - Pruhova, Stepanka

AU - Andersson, Ehm A

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

PY - 2010/1/1

Y1 - 2010/1/1

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.

KW - Diabetes Mellitus, Type 1

KW - Diabetes Mellitus, Type 2

KW - Diabetes, Gestational

KW - Female

KW - Genetic Variation

KW - Humans

KW - Insulin

KW - Male

KW - Mutation

KW - Pedigree

KW - Phenotype

KW - Pregnancy

KW - Young Adult

U2 - 10.1186/1471-2350-11-42

DO - 10.1186/1471-2350-11-42

M3 - Journal article

C2 - 20226046

VL - 11

SP - 42

JO - B M C Medical Genetics

JF - B M C Medical Genetics

SN - 1471-2350

ER -

ID: 34076391