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Down syndrome (DS) is the most common genetically defined cause of intellectual disabilities.
Cystic fibrosis is one of the most common genetically inherited diseases in Northern Europe, consisting of an inherited defect of chloride transport in the epithelium.
Cystic fibrosis is one of the most common genetically inherited diseases in Northern Europe, consisting of a defect of chloride transport in the epithelium, with the DF508 mutation being the most common mutation associated with the disease.
Currently, the most common genetically modified mammalian model is the mouse.
Cystic fibrosis is the most common genetically determined, life-limiting disorder in populations of European ancestry.
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This gene-paucity, they reckon, is why chromosome 21 is associated with Down's syndrome, the most common form of genetically mediated mental retardation.
Fragile X is the most common form of genetically inherited mental retardation.
Stargardt disease is the most common form of genetically driven progressive juvenile macular degeneration that affects central vision.
Ultimately, research consortiums incorporating animal models and well-characterized clinical populations will be necessary to fully understand the natural history of the c9FTD/ALS clinical phenotypes and identify biomarkers and therapeutic agents that can cure the most common form of genetically determined FTD and ALS.
Spinal Muscular Atrophy (SMA) is the second most common autosomal recessive genetic disease in humans and is the leading cause of genetically linked infant mortality, with an incidence rate of approximately 1 in 6000 births [1], [2], [3].
According to the United Nations AIDS program, two types of H.I.V. are currently recognized, and the most common, H.I.V.-1, has 10 genetically distinct subtypes.
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