1 Einträge von mit visual mutations
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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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visual loss, 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 major sy mutations are related to LCA; these are often found in both copies of the gene in each chromosome of the homologous chromosome pair (biallelic mutations). LCA’s clinical symptoms are diverse, including low light sensitivity (photo
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extern (outbound) Link/Domain 2 in .clinicalodyssey.com
intern (inbound) Link/Domain .clinicalodyssey.com
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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 |
Alle Keywords (Suchwörter) Liste aller Einträge
Textauszug aus Quelle
visual loss, 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 major sy mutations are related to LCA; these are often found in both copies of the gene in each chromosome of the homologous chromosome pair (biallelic mutations). LCA’s clinical symptoms are diverse, including low light sensitivity (photo
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