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Q51756725-6AFFC360-C877-40F6-B33B-46B15AB25C35
Q51756725-6AFFC360-C877-40F6-B33B-46B15AB25C35
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51756725-6AFFC360-C877-40F6-B33B-46B15AB25C35
A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency.
P2860
Q51756725-6AFFC360-C877-40F6-B33B-46B15AB25C35
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51756725-6AFFC360-C877-40F6-B33B-46B15AB25C35
rank
NormalRank
type
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Statement
wasDerivedFrom
45699067bb97a99de76f3ff9ae9dc85064251c31
P2860
The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families