Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”

Josef Finsterer; Sinda Zarrouk-Mahjoub

doi:10.1161/CIRCGENETICS.116.001630

Journal articles

Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”

Josef Finsterer ¹ Sinda Zarrouk-Mahjoub ²

1 Krankenanstalt Rudolfstiftung

2 LR11IPT05 - Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory

Keywords : Genetics Echocardiography Imaging and Diagnostics Testing Genetics and Genomics Magnetic Resonance Imaging (MRI) Imaging and Nuclear Medicine

Document type :

Journal articles

Domain :

Life Sciences [q-bio] / Human health and pathology

Complete list of metadatas

https://hal-riip.archives-ouvertes.fr/pasteur-02058838
Contributor : Abdelhakim Ben Hassine <>
Submitted on : Wednesday, March 6, 2019 - 10:59:53 AM
Last modification on : Wednesday, May 15, 2019 - 11:20:08 AM

Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”

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Letter by Finsterer and Zarrouk-Mahjoub Regarding Article, “Combination of Whole Genome Sequencing, Linkage, and Functional Studies Implicates a Missense Mutation in Titin as a Cause of Autosomal Dominant Cardiomyopathy With Features of Left Ventricular Noncompaction”

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