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α‐tropomyosin gene (TPM3) mutation in an infant with nemaline myopathy
oleh: Sulaiman Almobarak, Jonathan Hu, Kristopher D. Langdon, Lee‐Cyn Ang, Craig Campbell
Format: | Article |
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Diterbitkan: | Wiley 2021-03-01 |
Deskripsi
Abstract We report a case of neonatal nemaline myopathy with a de novo TPM3 mutation, which has been classified as a likely pathogenic mutation. With the expanding use of genetic testing in congenital myopathies, genotype‐phenotype descriptions of novel variants are important to inform clinical care, diagnosis, genetic counseling, and management of disease.