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t/gene-dhcr7

DHCR7 gene

Discuss publications and research concerning the DHCR7 gene.

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Related literature

Global Genetic Variation in Circulating 25-Hydroxyvitamin D: A Systematic Review of GWAS Evidence Across Different Ancestral Groups.
DHCR7
A c.89G>C p.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith-Lemli-Opitz Syndrome.
DHCR7
Multiomic molecular patterns of lipid dysregulation in a subphenotype of sepsis with higher shock incidence and mortality.
DHCR7
Diagnostic challenge between a frequent polygenic hypocholesterolemia and an unusual Smith Lemli Opitz syndrome related to bi-allelic DHCR7 mutations.
DHCR7
Vulnerability of DHCR7+/- mutation carriers to aripiprazole and trazodone exposure.
DHCR7
No Association of Vitamin D Pathway Genetic Variants with Cancer Risks in a Population-Based Cohort of German Older Adults.
DHCR7
No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization study.
DHCR7
Sterols and oxysterols in plasma from Smith-Lemli-Opitz syndrome patients.
DHCR7
Germline genetics of cancer of unknown primary (CUP) and its specific subtypes.
DHCR7
The p.Phe174Ser mutation is associated with mild forms of Smith Lemli Opitz Syndrome.
DHCR7

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