Ornithine aminotransferase (OAT), a mitochondrial matrix enzyme, is deficient in patients with gyrate atrophy of the choroid and retina. In human, the OAT structural gene maps to Chromosome (Chr) 10q26 and several OAT-related sequences, some of which are known to be processed pseudogenes, which map
โฆ LIBER โฆ
Chromosomal mapping of glutamate dehydrogenase gene sequences to mouse chromosomes 7 and 14
โ Scribed by Tzimagiorgis, George; Adamson, M.Charlene; Kozak, Christine A.; Moschonas, Nicholas K.
- Book ID
- 123053732
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- English
- Weight
- 935 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0888-7543
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