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.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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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.

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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.

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

@en

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

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P1476

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

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P2093

Alessandra Tessa

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Alexandra Durr

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Christelle Tesson

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Claire Pujol

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Cyril Goizet

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Daniel Mansuy

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François Rivier

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Giovanni Benard

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Guillaume Banneau

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Isabelle Coupry

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P2860

CYP2U1 mutations in two Iranian patients with activity induced dystonia, motor regression and spastic paraplegia.

Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology

CYP2U1, a novel human thymus- and brain-specific cytochrome P450, catalyzes omega- and (omega-1)-hydroxylation of fatty acids

Automated docking of flexible ligands: applications of AutoDock

Role of cytochrome P450 enzymes in the bioactivation of polyunsaturated fatty acids

Cytochrome P450 eicosanoids and cerebral vascular function

SIFT: Predicting amino acid changes that affect protein function

AutoDock4 and AutoDockTools4: Automated docking with selective receptor flexibility

Evaluation of comparative protein modeling by MODELLER

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms.

P304

140-151

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P31

scholarly article

P356

10.1002/HUMU.23359

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P433

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P478

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P50

P577

2017-11-11T00:00:00Z

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P698

29034544

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