Fragile X CGG expansion detection

GenoLife
Caja de Fragile X CGG expansion detection

Delivery time

Resultados: 5 semanas desde la recepción de la muestra

Sample

Hisopo bucal o saliva; Sangre

1.032,00€
Caja de Fragile X CGG expansion detection

Fragile 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.

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