EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome.
Delépine, M
EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. [electronic resource] - Nature genetics Aug 2000 - 406-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1061-4036
10.1038/78085 doi
Abnormalities, Multiple--genetics
Amino Acid Sequence
Base Sequence
DNA--chemistry
DNA Mutational Analysis
Diabetes Mellitus, Type 1
Epiphyses--abnormalities
Family Health
Female
Gene Frequency
Genotype
Growth Disorders
Haplotypes
Humans
Infant
Male
Microsatellite Repeats
Molecular Sequence Data
Mutation
Pedigree
Polymorphism, Genetic
Sequence Homology, Amino Acid
Syndrome
eIF-2 Kinase--genetics
EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. [electronic resource] - Nature genetics Aug 2000 - 406-9 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1061-4036
10.1038/78085 doi
Abnormalities, Multiple--genetics
Amino Acid Sequence
Base Sequence
DNA--chemistry
DNA Mutational Analysis
Diabetes Mellitus, Type 1
Epiphyses--abnormalities
Family Health
Female
Gene Frequency
Genotype
Growth Disorders
Haplotypes
Humans
Infant
Male
Microsatellite Repeats
Molecular Sequence Data
Mutation
Pedigree
Polymorphism, Genetic
Sequence Homology, Amino Acid
Syndrome
eIF-2 Kinase--genetics