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&ast;These authors contributed equally to the work

CYP2D6 as a treatment decision aid for ER-positive non-metastatic breast cancer patients: a systematic review with accompanying clinical practice guidelines
Glutaminase deficiency caused by short tandem repeat expansion in GLS
Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis
Association between SLC16A5 genetic variation and cisplatin-induced ototoxic effects in adult patients with testicular cancer
Identification of a large intronic transposal insertion in SLC17A5 causing sialic acid storage disease
CYP2B6*6 and CYP2B6*18 predict long-term efavirenz exposure measured in hair samples in HIV-positive South African women
Characterization of the genetic variation present in CYP3A4 in three South African populations
Extended haplotype studies in South African and Dutch variegate porphyria families carrying the recurrent p.R59W mutation confirm a common ancestry

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