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Iranian Red Crescent Medical Journal, ISSN 2074-1804, 01/2017, Volume 19, Issue 1, p. 1
Background: Multiple sclerosis (MS) is an autoimmune disease that affects the central nervous system (CNS). MS is one of the most common cause of neurological... 
Multiple sclerosis | Autoimmune diseases | FOXP3 | Genetic polymorphisms | Multiple Sclerosis | MEDICINE, GENERAL & INTERNAL | TARGET GENES | STIMULATION | Autoimmune Diseases | TRANSCRIPTION FACTOR FOXP3 | REGULATORY T-CELLS | SUPPRESSOR FUNCTION | PREECLAMPSIA | POLYMORPHISM | Genetic Polymorphisms
Journal Article
Genetic Testing and Molecular Biomarkers, ISSN 1945-0265, 08/2017, Volume 21, Issue 8, pp. 485 - 490
Journal Article
Ophthalmic genetics, 06/2019, p. 1
: Cone-rod dystrophy (CRD) is an inherited retinal dystrophy that is transmitted via different modes of inheritance. Mutations in more than 30 genes have been... 
Journal Article
Ophthalmic Genetics, ISSN 1381-6810, 05/2019, Volume 40, Issue 3, pp. 259 - 266
Purpose: Cone-rod dystrophy (CRD) is an inherited retinal dystrophy that is transmitted via different modes of inheritance. Mutations in more than 30 genes... 
incomplete penetrance | autosomal recessive inheritance pattern | Cone-rod dystrophy | CRX gene | GENETICS & HEREDITY | OPHTHALMOLOGY | MUTATIONS | HOMEOBOX GENE | ABCA4 GENE
Journal Article
Journal of Neural Transmission, ISSN 0300-9564, 3/2016, Volume 123, Issue 3, pp. 323 - 328
Journal Article
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