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—Familial hypertrophic cardiomyopathy (HCM) is caused by mutations in at least 8 contractile protein genes, most commonly ␤ myosin heavy chain, myosin binding protein C, and cardiac troponin T. Affected individuals are heterozygous for a particular mutation, and most evidence suggests that the mutant protein acts in a dominant-negative fashion. To(More)
Aim of this study was to investigate at what age German children master prosodic and morphological constraints in the acquisition of the word formation paradigm -heit/-keit, which is comparable to English -ness, and whether children with Specific Language Impairment (SLI) have difficulties identifying the prosodic cues from the input. Derived words with(More)
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