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  3. Supplementary data for: A novel POR G88S mutation causes severe PORD and establishes a critical pharmacogenomic risk profile

Supplementary data for: A novel POR G88S mutation causes severe PORD and establishes a critical pharmacogenomic risk profile

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Project description
Supplementary data for: A novel POR G88S mutation causes severe PORD and establishes a critical pharmacogenomic risk profile
Data Availability
Open
Contact Person
Pandey, Amit Vikram  
Department of Paediatrics  
Author(s)
Pandey, Amit Vikram  
Department of Paediatrics  
DOI
10.48620/91916
Organization(s)
Department of Paediatrics  
Languages
en
Subject(s)
500 Science > 570 Life sciences; biology
600 Technology > 610 Medicine & health
Subjects
P450
•
P450 reductase
•
PORD
Rights URI
Attribution (CC BY 4.0)
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