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Genetic architecture and adaptations of Nunavik Inuit - Dataset
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Genetic architecture and adaptations of Nunavik Inuit - Dataset
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A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese fami...
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Genetic architecture and adaptations of Nunavik Inuit
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Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nun...
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Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nun...
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Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nun...
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Increased Missense Mutation Burden of Fatty Acid Metabolism Related Genes in Nun...
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Mutations in the nervous system–specific HSN2 exon of WNK1 cause hereditary sens...
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A VAMP1 Mutation Causes Chromosome 12p13 Hereditary Spastic Ataxia in Newfoundla...
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Genome-wide association analysis identifies new candidate risk loci for familial...
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CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height...
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CPT1A Missense Mutation Associated with Fatty Acid Metabolism and Reduced Height...
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A stop codon mutation in SCN9A causes lack of pain sensation
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A stop codon mutation in SCN9A causes lack of pain sensation
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A stop codon mutation in SCN9A causes lack of pain sensation
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VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Familie...
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VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Familie...
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Identification of a Novel Gene (HSN2) Causing Hereditary Sensory and Autonomic N...
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Life-threatening viral disease in a novel form of autosomal recessive IFNAR2 def...
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