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Journal of Human Genetics and Genomics
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Volume 2, Number 1 (2018-7)
Novel Homozygous Nonsense Mutation of PMS1 in a Patient with Multifocal Schwanomatosis Schwanomatosis Resembling Neurofibromatosis Type 2
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A Novel Mutation in TMPRSS15 Gene Causes a Severe Form of Congenital Enterokinase Deficiency
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Considering Exososomal MicroRNAs as Biomarkers in Multiple Sclerosis
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Hemophilia Gene Therapy; Clinical and Molecular Aspects
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Rs214101 Variation of NUCB2/Nesfatin-1 Gene: Effects on Metabolic Parameters Independent of Type 2 Diabetes or Obesity in Coronary Artery Disease
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The Most Well - known Markers of CSCs and Their Role in Growth of Tumors, Drug Resistance and Metastasis
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