Clinical RNA sequencing confirms compound heterozygous intronic variants in RYR1 in a patient with congenital myopathy, respiratory failure, neonatal brain hemorrhage, and d‐transposition of the great arteries
Abstract Background Defects in the RYR1 (OMIM#180901) gene lead to Ryanodine receptor type 1‐related myopathies (RYR1‐RM); the most common subgroup of congenital myopathies. Methods Congenital myopathy presents a diagnostic challenge due to the need for multiple testing modalities to identify the ma...
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| Auteurs principaux: | , , , , , , |
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| Format: | article |
| Langue: | EN |
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Wiley
2021
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| Accès en ligne: | https://doaj.org/article/591293b797094854879f0af6d396af3c |
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