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Genotype phenotype analysis in a family carrying truncating mutations in the titin gene
We report a family carrying a previously described truncating mutation, NM_001267550.2(TTN):c.107889del p.(Lys35963Asnfs*9) in exon 364, and a novel truncating mutation, NM_001267550.1:c.100704C > A p.(Tyr33568*) in exon 358 in the titin gene. The c.107889del mutation, which was maternally transm...
Bewaard in:
| Gepubliceerd in: | Acta Myol |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Pacini Editore Srl
2021
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8033428/ https://ncbi.nlm.nih.gov/pubmed/33870097 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.36185/2532-1900-043 |
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