Population
9 Palestinian patients from 7 unrelated families who have nemaline myopathy
Design
Case_series
Authors
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Identifies TNNT1 mutations in non-Amish patients; extends the genetic spectrum but leaves open prevalence and phenotype correlations.
Identifies a novel TNNT1 mutation causing nemaline myopathy, expanding the known genetic and phenotypic spectrum of the disease.
Abdulhaq et al. (2015) studied this question.
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