Disorders

TNNT2-Related Familial Restrictive Cardiomyopathy

Synonym(s): Familial Restrictive Cardiomyopathy 3, RCM3

Gene	Locus	Protein
TNNT2	1q32	Troponin T, cardiac muscle

Laboratory	Test Method	Prenatal	Carrier *
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany	• Sequence analysis of the entire coding region
Health in Code S.L. - A Coruña, Spain	• Sequence analysis of the entire coding region
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain	• Sequence analysis of the entire coding region
University Hospital Münster, Institute for Genetics of Heart Diseases (IfGH) - Münster, Germany	• Sequence analysis of the entire coding region

^* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.