Ads
-
Related paper
- Assessment of Mutation Genetics in HTT (Hi-CAG), Gene for Induced Huntington’s disease in Tabriz, Iran
- Study of Genetics Mutations in HEXA Gene for Induced Tay-Sachs Disease in Human, Tabriz, Iran
- HUNTINGTON'S DISEASE: UNDERSTANDING THE PATHOPHYSIOLOGY THROUGH THE HUNTINGTIN GENE
- FREQUENCY OF R1193Q MUTATION IN SCNSA GENE ON SUSCEPTIBILITY FOR ARVC AND LQTS IN IRAN
- A Novel Mutation in the PYGM Gene Resulting in Mcardle Disease
- One Case Report and Literature Review of Alexander’s Disease Caused by a Mutation in the GFAP Gene | Biomedgrid LLC
- EVALUATING NEUROPROTECTIVE EFFECTS OF ASCORBIC ACID AGAINST 3- NITROPROPIONIC ACID INDUCED HUNTINGTON’S DISEASE IN RATS: POSSIBLE INVOLVEMENT OF GABAARECEPTORS
- EVALUATING NEUROPROTECTIVE EFFECTS OF ASCORBIC ACID AGAINST 3- NITROPROPIONIC ACID INDUCED HUNTINGTON’S DISEASE IN RATS: POSSIBLE INVOLVEMENT OF GABAARECEPTORS
- Identification of compound heterozygosity for a rare beta-globin gene mutation, codon 15 (-T) with a common mutation IVS1-5 (G>C) by direct sequencing in a Bangladeshi patient
- Construction of Indonesian-Strain Avian Flu Virus Seed Vaccine Using Low Pathogenic Hemagglutinin Gene and Neuraminidase Pr8 Gene through Reverse Genetics