Alkaptonuria (aku), an inborn error of metabolism caused by the loss of homogentisate 1,2dioxygenase (HGD), has been described in a mouse model created by ethylnitrosourea mutagenesis but the mutation in these mice has not previously been identified. We used RT-PCR to amplify the Hgd cDNA from Hgd a
Alkaptonuria in the Trenčín District of Czechoslovakia
✍ Scribed by Sršeň, Štefan ;Cisárik, František ;Pásztor, Ladislav ;Harmečko, Ladislav ;Opitz, John M.
- Publisher
- John Wiley and Sons
- Year
- 1978
- Tongue
- English
- Weight
- 317 KB
- Volume
- 2
- Category
- Article
- ISSN
- 0148-7299
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