Reactome | CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

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CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5 Show undefined attributes

author	[Person:5602239] Goizet, C [Person:5602932] Boukhris, A [Person:5602211] Durr, A [Person:5603009] Beetz, C [Person:5602835] Truchetto, J [Person:5602218] Tesson, C [Person:5602930] Tsaousidou, M [Person:5602882] Forlani, S [Person:5602182] Guyant-Mar�chal, L [Person:5603002] Fontaine, B [Person:5602912] Guimar�es, J [Person:3322924] Isidor, B [Person:5602904] Chazouill�res, O [Person:5602939] Wendum, D [Person:3785722] Grid, D [Person:5602843] Chevy, F [Person:5602977] Chinnery, PF [Person:5602834] Coutinho, P [Person:5602839] Azulay, JP [Person:5602954] Feki, I [Person:5602215] Mochel, F [Person:5602907] Wolf, C [Person:5602947] Mhiri, C [Person:5602963] Crosby, A [Person:5602247] Brice, A [Person:5602258] Stevanin, G
created	[InstanceEdit:5602968] Jassal, Bijay, 2014-06-25
dbId	5602916
displayName	CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
journal	Brain
pages	1589-600
pubMedIdentifier	19439420
schemaClass	LiteratureReference
title	CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5
url	http://www.ncbi.nlm.nih.gov/pubmed/19439420
volume	132
year	2009

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[FailedReaction:R-HSA-5602885] Defective CYP7B1 does not 7-hydroxylate 25OH-CHOL

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