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CYP7B1 wt Allele

Known as: CP7B, SPG5A, Cytochrome P450, Subfamily VIIB (Oxysterol 7 Alpha-Hydroxylase), Polypeptide 1 Gene 
Human CYP7B1 wild-type allele is located in the vicinity of 8q21.3 and is approximately 211 kb in length. This allele, which encodes 25… 
National Institutes of Health

Related topics

Related topics

8 relations
Bile Acid Biosynthesis PathwayIron ChelationLipid MetabolismMetabolic Detoxication, Drug

Papers overview

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2012
2012
CYP7B1 Mutations in French-Canadian Hereditary Spastic Paraplegia Subjects
Lorrain disease, refers to progressive motor neurodegenerative disorders characterized by lower limb spasticity and weakness… 
2002
2002
Confirmation and refinement of the SPG5A locus for pure autosomal recessive hereditary spastic paraplegia.
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