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Patient perspective: my rare disease journey
My underlying diagnosis since birth was congenital muscular dystrophy not otherwise specified. Being born in 1970 meant that there were no genetic testing, no standards of care, and no true understanding of the pathology that separates one congenital-onset neuromuscular disorder from the next. Two m...
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Cold Spring Harbor Laboratory Press
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8958917/ https://www.ncbi.nlm.nih.gov/pubmed/35217566 http://dx.doi.org/10.1101/mcs.a006205 |