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Mutation in the PCSK9 gene in Omani Arab subjects with autosomal dominant hypercholesterolemia and its effect on PCSK9 protein structure
Oman Medical Journal. 2013; 28 (1): 48-52
in En | IMEMR | ID: emr-146731
Responsible library: EMRO
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Index: IMEMR Main subject: Chromosome Disorders / Proprotein Convertase 2 / Genes, Dominant / Hypercholesterolemia / Cholesterol, LDL / Mutation Type of study: Case_reports Limits: Female / Humans / Male Language: En Journal: Oman Med. J. Year: 2013
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Index: IMEMR Main subject: Chromosome Disorders / Proprotein Convertase 2 / Genes, Dominant / Hypercholesterolemia / Cholesterol, LDL / Mutation Type of study: Case_reports Limits: Female / Humans / Male Language: En Journal: Oman Med. J. Year: 2013