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GO:0005861troponin complexPMID:9060892IMP: Inferred from Mutant Phenotype C
This annotation made on page:
By: Bhatt001 (group Team The Histones) on 2012-02-25 19:34:25 CST.




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Entry TypeChallenging User,GroupTime/DateChallenge ReasonPoints/Assessment
ChallengeBurks004,
Team Cancer Dancers
2012-02-29 19:06:51 CST

The article Sudden Death due to Troponin T Mutations PMID:9060892 table 2, displays the clinical features of associated with hypertrophic cardiomyopathy in 2 pedigrees. The mutant they refer to is an arginine 92 tryptophan mutation while Troponin complex (GO:0005861) refers to a complex consisting of three different subunits – troponin T (TnT), troponin I (TnI) and troponin C (TnC).

2
Private
Assessment
Streptoman2012-02-28 19:46:57 CSTYou need to be an instructor to view these notes.Unacceptable