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Novel compound heterozygous TTN variants as a cause of severe neonatal congenital contracture syndrome without cardiac involvement diagnosed with rapid trio exome sequencing

Helen McDermott, Amy Henderson, Hannah K. Robinson, Richard Heaver, Chrisantha Halahakoon, Helen Cox, Swati Naik

2021Neuromuscular Disorders13 citationsDOI

Topics & Concepts

ArthrogryposisExome sequencingCompound heterozygosityHypotoniaNonsenseFrameshift mutationProbandGeneticsExonMedicineMuscle HypotoniaPhenotypeBiologyGeneMutationCardiomyopathy and Myosin StudiesNeurogenetic and Muscular Disorders ResearchMuscle Physiology and Disorders
Novel compound heterozygous TTN variants as a cause of severe neonatal congenital contracture syndrome without cardiac involvement diagnosed with rapid trio exome sequencing | Litcius