2 Einträge von 2 mit gene lack
clinicalodyssey.com
Datum der Indexierung 03.05.2024 22:10:02
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Kombination Keywords gene lack | retinal your | light particles | clinical reactions | therapy vision | that inherited | cells test | visual viral | patient protein | into this |
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Gene therapy: Leber Congenital Amaurosis Background Fact Explanation Inherited retinal diseases Inherited retinal diseases are a group of genetic conditions that cause degradation of the light-sensitive cells in the retina. Frequently progressive and lack of pupillary light reflex (amaurotic pupils), nystagmus, and a lack of electrical signs on electroretinogram. Nystagmus is generally the first sign, apparent at the age of 6 weeks. LCA is a form of retinal dystrophy without m
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Kombination Keywords gene lack | retinal your | light particles | clinical reactions | therapy vision | that inherited | cells test | visual viral | patient protein | into this |
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Gene therapy: Leber Congenital Amaurosis Background Fact Explanation Inherited retinal diseases Inherited retinal diseases are a group of genetic conditions that cause degradation of the light-sensitive cells in the retina. Frequently progressive and lack of pupillary light reflex (amaurotic pupils), nystagmus, and a lack of electrical signs on electroretinogram. Nystagmus is generally the first sign, apparent at the age of 6 weeks. LCA is a form of retinal dystrophy without m
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clinicalodyssey.com
Datum der Indexierung 03.05.2024 22:09:36
erkannte Namen Gene Therapy |
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Kombination Keywords gene number | from muscular | this type | protein produced | deletion mrna | with have | clinical motor | exon patients | therapy disease | copies onset |
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Gene Therapy: Spinal Muscular Atrophy Background Fact Explanation Spinal muscular atrophy (SMA) Spinal muscular atrophy (SMA) refers to a group of rare genetic diseases, many of which are caused by deletions or mutations in both copies of the surviva lack of the SMN protein. This results in impaired motor neuron function by degeneration of the spinal anterior horn cells (alpha motor neurons). Loss of functional motor neurons causes severe, progressive muscle atrophy and weakne
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erkannte Namen Gene Therapy |
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Kombination Keywords gene number | from muscular | this type | protein produced | deletion mrna | with have | clinical motor | exon patients | therapy disease | copies onset |
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Gene Therapy: Spinal Muscular Atrophy Background Fact Explanation Spinal muscular atrophy (SMA) Spinal muscular atrophy (SMA) refers to a group of rare genetic diseases, many of which are caused by deletions or mutations in both copies of the surviva lack of the SMN protein. This results in impaired motor neuron function by degeneration of the spinal anterior horn cells (alpha motor neurons). Loss of functional motor neurons causes severe, progressive muscle atrophy and weakne
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