Pages that link to "Q28237918"

The following pages link to Identification of new mutations in sterol 27-hydroxylase gene in Japanese patients with cerebrotendinous xanthomatosis (CTX) (Q28237918):

Displaying 12 items.

• Fine-mapping, mutation analyses, and structural mapping of cerebrotendinous xanthomatosis in U.S. pedigrees (Q28350244) (← links)
• Atherosclerosis and sterol 27-hydroxylase: evidence for a role of this enzyme in elimination of cholesterol from human macrophages (Q28369414) (← links)
• Diagnosis of inherited metabolic disorders affecting the nervous system (Q33734674) (← links)
• A novel mutation in the sterol 27-hydroxylase gene of a woman with autosomal recessive cerebrotendinous xanthomatosis. (Q34220748) (← links)
• Mutations producing premature termination of translation and an amino acid substitution in the sterol 27-hydroxylase gene cause cerebrotendinous xanthomatosis associated with parkinsonism (Q35452383) (← links)
• Review of progress in sterol oxidations: 1987-1995. (Q41051532) (← links)
• Frontal lobe dementia with abnormal cholesterol metabolism and heterozygous mutation in sterol 27-hydroxylase gene (CYP27). (Q43696621) (← links)
• A Case of Late-onset Cerebrotendinous Xanthomatosis with a Novel Mutation in the CYP27A1 Gene (Q50055916) (← links)
• CYP27A1 does not 27-hydroxylate 5bCHOL3a,7a,12a-triol (Q50289153) (← links)
• 27-Hydroxycholesterol Is an Estrogen Receptor β-Selective Negative Allosteric Modifier of 17β-Estradiol Binding. (Q52341734) (← links)
• Defective CYP27A1 does not 27-hydroxylate 5β-CHOL3α,7α,24(s)-triol (Q55214612) (← links)
• Usefulness of comprehensive targeted multigene panel sequencing for neuromuscular disorders in Korean patients (Q93050552) (← links)