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Detects mitochondrial DNA mutations linked to Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
11,025 THB
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Detects mitochondrial DNA mutations associated with Leber hereditary optic neuropathy (LHON).
7,455 THB
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Detects mutations in mitochondrial DNA linked to MELAS, MERRF, and NARP syndromes.
7,245 THB
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Detects mutations in the dysferlin gene associated with muscular dystrophy (dysferlinopathy).
38,400 THB
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Detects Entamoeba histolytica DNA, used to diagnose amoebic dysentery or liver abscess.
6,900 THB
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Sequencing of the entire exome to identify genetic causes for undiagnosed conditions.
105,000 THB
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Detects mutations in the FGFR2 gene, used to diagnose craniosynostosis syndromes like Apert syndrome.
7,245 THB
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Detects mutations in the FGFR3 gene, associated with achondroplasia and other skeletal disorders.
7,245 THB
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