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Publications by Romain Clement

Trafficking Defective Mutations Modulate NaV1.5 N—Glycosylation States

Biophysical Journal

English

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TBC1D8B Loss-Of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways

American Journal of Human Genetics

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Congenital Hyperinsulinism Associated ABCC8 Mutations That Cause Defective Trafficking of ATP-Sensitive K+ Channels: Identification and Rescue

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Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel

Frontiers in Physiology

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Defective Potassium Channel Kir2.1 Trafficking Underlies Andersen-Tawil Syndrome

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Congenital Disorders of Glycosylation. Part I. Defects of Protein N-Glycosylation.

Acta Biochimica Polonica

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Clinical Utility Gene Card For: GALNT3 Defective Congenital Disorder of Glycosylation

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Inactivating BRAF Mutations Modulate RAS–MAPK Signaling

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The Interaction Between the First Transmembrane Domain and the Thumb of ASIC1a Is Critical for Its N-Glycosylation and Trafficking

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Mechanism of Carbamazepine Mediated Rescue of Trafficking Defective Mutant KATP Channels

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