Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

@en

Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

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P1476

Mutations in CYB561 Causing a Novel Orthostatic Hypotension Syndrome.

@en

P2093

Arjan P M de Brouwer

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Gerjan Navis

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Gert Jan Luijckx

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Herman H W Silljé

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Ido P Kema

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Irene Mateo Leach

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Italo Biaggioni

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J Peter van Tintelen

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Jan D H Jongbloed

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Marc H Hemmelder

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P2860

Congenital dopamine-beta-hydroxylase deficiency. A novel orthostatic syndrome

Structure and mechanism of a eukaryotic transmembrane ascorbate-dependent oxidoreductase

Large Neutral Amino Acid Supplementation Exerts Its Effect through Three Synergistic Mechanisms: Proof of Principle in Phenylketonuria Mice

The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data

Isolated failure of autonomic noradrenergic neurotransmission. Evidence for impaired beta-hydroxylation of dopamine.

Catecholamine pathway gene variation is associated with norepinephrine and epinephrine concentrations at rest and after exercise.

Characterization of Disease-Associated Mutations in Human Transmembrane Proteins

Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected]

Cytochromes b561: ascorbate-mediated trans-membrane electron transport.

Monoamine neurotransmitter disorders--clinical advances and future perspectives.

P304

846-854

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P31

scholarly article

P356

10.1161/CIRCRESAHA.117.311949

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P433

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P478

122

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P50

Ron A. Wevers

Hanka Venselaar

Maarten P van den Berg

P577

2018-01-17T00:00:00Z

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P698

29343526

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P932

5924476

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