TY  - GEN
AU  - Svalastoga,Pernille
AU  - Sulen,Åsta
AU  - Fehn,Jarle R
AU  - Aukland,Stein M
AU  - Irgens,Henrik
AU  - Sirnes,Eivind
AU  - Fevang,Silje K E
AU  - Valen,Eivind
AU  - Elgen,Irene B
AU  - Njølstad,Pål R
TI  - Intellectual Disability in K
SN  - 1935-5548
PY  - 2020///1201
KW  - Adolescent
KW  - Amino Acid Substitution
KW  - Case-Control Studies
KW  - Child
KW  - Child, Preschool
KW  - Codon, Nonsense
KW  - Cohort Studies
KW  - Diabetes Mellitus, Type 1
KW  - complications
KW  - Female
KW  - Genetic Association Studies
KW  - Genotype
KW  - Humans
KW  - Infant, Newborn
KW  - Infant, Newborn, Diseases
KW  - genetics
KW  - Intellectual Disability
KW  - epidemiology
KW  - Male
KW  - Methionine
KW  - Mutation, Missense
KW  - Norway
KW  - Potassium Channels, Inwardly Rectifying
KW  - Sulfonylurea Receptors
KW  - Valine
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.2337/dc19-1013
ER  -