TTR gene mutation; transthyretin gene mutation
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Clinical significance
- defects in transthyretin (TTR) are the cause of
- see transthyretin
More general terms
Additional terms
References
- ↑ Loinc
- ↑ ARUP Consult: Familial Transthyretin Amyloidosis (TTR) Sequencing https://arupconsult.com/ati/familial-transthyretin-amyloidosis-ttr-sequencing