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Copper-dependent interaction of glutaredoxin with the N termini of the copper-ATPases (ATP7A and ATP7B) defective in Menkes and Wilson diseases

โœ Scribed by Chris M. Lim; Michael A. Cater; Julian F.B. Mercer; Sharon La Fontaine

Book ID
116293340
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
362 KB
Volume
348
Category
Article
ISSN
0006-291X

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โœ Gloria Hsi; Lara M. Cullen; Georgina Macintyre; Matthew M. Chen; D. Moira Glerum ๐Ÿ“‚ Article ๐Ÿ“… 2008 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 457 KB ๐Ÿ‘ 1 views

ATP7B is a copper transporting P-type ATPase defective in the autosomal recessive copper storage disorder, Wilson disease (WND). Functional assessment of variants helps to distinguish normal from disease-causing variants and provides information on important amino acid residues. A total of 11 missen