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  2. Details for: CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56.
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CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56. [electronic resource]

By:
  • Durand, Christelle M
Contributor(s):
  • Dhers, Laura
  • Tesson, Christelle
  • Tessa, Alessandra
  • Fouillen, Laetitia
  • Jacqueré, Stéphanie
  • Raymond, Laure
  • Coupry, Isabelle
  • Benard, Giovanni
  • Darios, Frédéric
  • El-Hachimi, Khalid H
  • Astrea, Guja
  • Rivier, François
  • Banneau, Guillaume
  • Pujol, Claire
  • Lacombe, Didier
  • Durr, Alexandra
  • Babin, Patrick J
  • Santorelli, Filippo M
  • Pietrancosta, Nicolas
  • Boucher, Jean-Luc
  • Mansuy, Daniel
  • Stevanin, Giovanni
  • Goizet, Cyril
Producer: 20180717Description: 140-151 p. digitalISSN:
  • 1098-1004
Subject(s):
  • Alleles
  • Amino Acid Substitution
  • Cytochrome P450 Family 2 -- chemistry
  • DNA Mutational Analysis
  • Enzyme Activation
  • Gene Expression
  • Genetic Association Studies
  • HEK293 Cells
  • Humans
  • Models, Molecular
  • Mutation, Missense
  • Oxidation-Reduction
  • Phenotype
  • Protein Conformation
  • Spastic Paraplegia, Hereditary -- diagnosis
Online resources:
  • Available from publisher's website
In: Human mutation vol. 39
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56.

APA

Durand C. M., Dhers L., Tesson C., Tessa A., Fouillen L., Jacqueré S., Raymond L., Coupry I., Benard G., Darios F., El-Hachimi K. H., Astrea G., Rivier F., Banneau G., Pujol C., Lacombe D., Durr A., Babin P. J., Santorelli F. M., Pietrancosta N., Boucher J., Mansuy D., Stevanin G. & Goizet C. (20180717). CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56. : Human mutation.

Chicago

Durand Christelle M, Dhers Laura, Tesson Christelle, Tessa Alessandra, Fouillen Laetitia, Jacqueré Stéphanie, Raymond Laure, Coupry Isabelle, Benard Giovanni, Darios Frédéric, El-Hachimi Khalid H, Astrea Guja, Rivier François, Banneau Guillaume, Pujol Claire, Lacombe Didier, Durr Alexandra, Babin Patrick J, Santorelli Filippo M, Pietrancosta Nicolas, Boucher Jean-Luc, Mansuy Daniel, Stevanin Giovanni and Goizet Cyril. 20180717. CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56. : Human mutation.

Harvard

Durand C. M., Dhers L., Tesson C., Tessa A., Fouillen L., Jacqueré S., Raymond L., Coupry I., Benard G., Darios F., El-Hachimi K. H., Astrea G., Rivier F., Banneau G., Pujol C., Lacombe D., Durr A., Babin P. J., Santorelli F. M., Pietrancosta N., Boucher J., Mansuy D., Stevanin G. and Goizet C. (20180717). CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56. : Human mutation.

MLA

Durand Christelle M, Dhers Laura, Tesson Christelle, Tessa Alessandra, Fouillen Laetitia, Jacqueré Stéphanie, Raymond Laure, Coupry Isabelle, Benard Giovanni, Darios Frédéric, El-Hachimi Khalid H, Astrea Guja, Rivier François, Banneau Guillaume, Pujol Claire, Lacombe Didier, Durr Alexandra, Babin Patrick J, Santorelli Filippo M, Pietrancosta Nicolas, Boucher Jean-Luc, Mansuy Daniel, Stevanin Giovanni and Goizet Cyril. CYP2U1 activity is altered by missense mutations in hereditary spastic paraplegia 56. : Human mutation. 20180717.

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