Restrictive Cardiomyopathy Resulting from a Troponin I Type 3 Mutation in a Chinese Family
Conclusion Using next generation sequencing, which has very recently been shown to be successful in identifying novel causative mutations of rare Mendelian disorders, we found a novel mutation of TNNI3 in a Chinese family with RCM.
Source: Chinese Medical Sciences Journal - Category: Journals (General) Source Type: research
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