Title : Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family.

Pub. Date : 1992 Jul

PMID : 1322359






1 Functional Relationships(s)
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1 We previously developed a DNA test based on amplification by the polymerase chain reaction followed by allele-specific oligonucleotide hybridization that identifies the base substitution adenine for guanine at nucleotide 654 in the gelsolin gene causing the disease. Adenine gelsolin Homo sapiens