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Publications by Samuel J. Gossage
Loss-Of-Function Mutations in Sodium Channel Nav1.7 Cause Anosmia
Nature
Multidisciplinary
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Homozygous Loss-Of-Function Mutations in SLC26A7 Cause Goitrous Congenital Hypothyroidism
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Loss-Of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome
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Sodium Channel, Voltage-Gated, Type IX, Α Subunit (SCN9A; NaV1.7)
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De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy
American Journal of Human Genetics
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Loss-Of-Function Mutations in UDP-Glucose 6-Dehydrogenase Cause Recessive Developmental Epileptic Encephalopathy
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Computational Study of the Loss-Of-Function Mutations in the Kv1.5 Channel Associated With Atrial Fibrillation
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Loss-Of-Function Mutations in QRICH2 Cause Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella
Nature Communications
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Mutations in NaV1.5 Reveal Calcium-Calmodulin Regulation of Sodium Channel
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Maturation of EEG Oscillations in Children With Sodium Channel Mutations
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