UDP-glucuronosyltransferase, Crigler-Najjar syndrome, CN1 and CN2
UDP-Glucuronosyl-Transferase, Crigler-Najjar-Syndrom, CN1 und CN2OMIM
191740
Gensymbole
UGT1A1
Material
EDTA-Blut: 1 - 2 ml
Methode
PCR und Sequenzierung der kodierenden Exons 1-5
Indication
Typ I: < 20 mg/dl (Serum Bilirubin)
Typ II: 20-50 mg/dl (Serum Bilirubin)
Accredited
yes
Contact person analyzes program
Dr. rer. nat. Thomas Haverkamp
Biologist Molecular Haemato-oncology, hereditary cancer syndromes- +49 231 9572-6617
- 0231 9572-86618