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Q35196805-A91FE163-BE29-42BD-ABBA-D96128AE9522
Q35196805-A91FE163-BE29-42BD-ABBA-D96128AE9522
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196805-A91FE163-BE29-42BD-ABBA-D96128AE9522
Finnish type of familial amyloidosis: cosegregation of Asp187----Asn mutation of gelsolin with the disease in three large families.
P2860
Q35196805-A91FE163-BE29-42BD-ABBA-D96128AE9522
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196805-A91FE163-BE29-42BD-ABBA-D96128AE9522
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
26313664014da650a2c35484d5cf5d1d4ab4b7ac
P2860
Variant apolipoprotein AI as a major constituent of a human hereditary amyloid