Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference11 articles.
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2. Gelsolin variant (Asn-187) in familial amyloidosis, Finnish type;Ghiso;Biochem. J.,1990
3. Localization of gelsolin proximal to ABL on chromosome 9;Kwiatkowski;Am. J. Hum. Genet.,1988
4. Mutation in gelsolin gene in Finnish hereditary amyloidosis;Levy;J. Exp. Med.,1990
5. Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): Relation of the amyloid protein to variant (Asn187) gelsolin;Maury;Biochim. Biophys. Acta,1990
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