{"product_id":"x-fragil-deteccion-de-la-expansion-cgg","title":"Fragile X CGG expansion detection","description":"\u003cp\u003eFragile X syndrome is the most common form of inherited intellectual disability. The disease is caused by a specific gene. Normally, the gene produces a protein needed for brain development. But a defect in this gene causes a person to produce little or no of that protein. This results in the symptom of fragile X.\u003c\/p\u003e","brand":"GenoLife","offers":[{"title":"1. Muestra extraída directamente en la clínica o centro solicitante [+0,00€] \/ Hisopo Bucal \/ Saliva","offer_id":52585000501514,"sku":"GENL-0038-07-1","price":1032.0,"currency_code":"EUR","in_stock":true},{"title":"1. Muestra extraída directamente en la clínica o centro solicitante [+0,00€] \/ Sangre EDTA","offer_id":52585000534282,"sku":"GENL-0038-07-2","price":1032.0,"currency_code":"EUR","in_stock":true}],"url":"https:\/\/www.genotica.com\/en\/products\/x-fragil-deteccion-de-la-expansion-cgg","provider":"Genotica","version":"1.0","type":"link"}