EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome. [electronic resource]
Producer: 20000828Description: 406-9 p. digitalISSN:- 1061-4036
- 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
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.