✦ LIBER ✦
Homozygous mutation Arg768Trp in the ABC-transporter encoding geneMRP2/cMOAT/ABCC2causes Dubin-Johnson syndrome in a Caucasian patient
✍ Scribed by Verena Materna; Hermann Lage
- Publisher
- Nature Publishing Group
- Year
- 2003
- Tongue
- English
- Weight
- 648 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1435-232X
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