Cytochrome P450 oxidoreductase deficiency caused by R457H mutation in POR gene in Chinese: case report and literature review. - Wikidata - awgldk - TriplyDB

Cytochrome P450 oxidoreductase deficiency caused by R457H mutation in POR gene in Chinese: case report and literature review.

Cytochrome P450 oxidoreductase deficiency caused by R457H mutation in POR gene in Chinese: case report and literature review.

http://www.wikidata.org/entity/Q37698004

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Cytochrome P450 oxidoreductase deficiency caused by R457H mutation in POR gene in Chinese: case report and literature review.

http://www.wikidata.org/entity/Q37698004

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 14 March 2017

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Cytochrome P450 oxidoreductase ...... report and literature review.

@en

Cytochrome P450 oxidoreductase ...... report and literature review.

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type

label

Cytochrome P450 oxidoreductase ...... report and literature review.

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Cytochrome P450 oxidoreductase ...... report and literature review.

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prefLabel

Cytochrome P450 oxidoreductase ...... report and literature review.

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Cytochrome P450 oxidoreductase ...... report and literature review.

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Cytochrome P450 oxidoreductase ...... report and literature review.

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Jinhui Li

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Xiaoli Wang

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Yang Bai

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Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acid

Diversity and function of mutations in p450 oxidoreductase in patients with Antley-Bixler syndrome and disordered steroidogenesis

Impaired hepatic drug and steroid metabolism in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency

Mutant P450 oxidoreductase causes disordered steroidogenesis with and without Antley-Bixler syndrome

Congenital adrenal hyperplasia caused by mutant P450 oxidoreductase and human androgen synthesis: analytical study

Backdoor pathway for dihydrotestosterone biosynthesis: implications for normal and abnormal human sex development

Prenatal diagnosis of P450 oxidoreductase deficiency (ORD): a disorder causing low pregnancy estriol, maternal and fetal virilization, and the Antley-Bixler syndrome phenotype

NADPH P450 oxidoreductase: structure, function, and pathology of diseases

Reduction in hepatic drug metabolizing CYP3A4 activities caused by P450 oxidoreductase mutations identified in patients with disordered steroid metabolism

Effects of genetic variants of human P450 oxidoreductase on catalysis by CYP2D6 in vitro

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