Title : Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.

Pub. Date : 1990 Dec 10

PMID : 2176164






1 Functional Relationships(s)
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1 Here we demonstrate, using polymerase chain reaction and allele-specific oligonucleotide hybridization analyses of genomic DNA, a single base mutation (G654----A654) in the gelsolin gene segment encoding the amyloid protein. Oligonucleotides gelsolin Homo sapiens