A novel non-sense mutation in the SLC2A10 gene of an arterial tortuosity syndrome patient of Kurdish origin. [electronic resource]
Producer: 20090819Description: 867-70 p. digitalISSN:- 1432-1076
- Abnormalities, Multiple -- genetics
- Arteries -- abnormalities
- Codon, Nonsense
- Connective Tissue -- abnormalities
- DNA Mutational Analysis
- Female
- Genes, Recessive
- Glucose Transport Proteins, Facilitative -- deficiency
- Hip Dislocation -- genetics
- Humans
- Infant
- Pedigree
- Phenotype
- Stomach -- abnormalities
- Syndrome
No physical items for this record
Publication Type: Case Reports; Journal Article
There are no comments on this title.
Log in to your account to post a comment.