Before scoliosis can be attributed to the variant c.326G>A in MYH3, its pathogenicity must be proven
Dear Editor, We were interested to read the article by Maccarone et al. about a 15-year-old girl with scoliosis, growth retardation, facial dysmorphism and delayed puberty.1 Genetic testing revealed the heterozygous variant NM_002470.4(MYH3):c.326G>A (p.Arg109His) in MYH3. The patient benefit...
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Format: | Article |
Language: | English |
Published: |
PAGEPress Publications
2025-06-01
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Series: | European Journal of Translational Myology |
Subjects: | |
Online Access: | https://www.pagepressjournals.org/bam/article/view/13832 |
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