Molecular genetic diagnosis of hereditary transthyretin amyloidosis (TTR gene)

Transthyretin amyloidosis is the most common form of hereditary (familial) amyloidosis. The disease is associated with abnormalities of the transthyretin protein encoded by the TTR gene. Clinical forms of this disease include familial amyloid cardiomyopathy, familial amyloid polyneuropathy, and senile familial amyloidosis.

Within 10 days. The specified time does not include the day of biomaterial collection