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Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1
| Formato: | Online Artículo Texto |
|---|---|
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014444/ https://www.ncbi.nlm.nih.gov/pubmed/29932520 http://dx.doi.org/10.1002/mgg3.418 |
| _version_ | 1783334234059964416 |
|---|---|
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6014444 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2018 |
| publisher | John Wiley and Sons Inc. |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-60144442018-07-05 Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1 Mol Genet Genomic Med Corrigendum John Wiley and Sons Inc. 2018-06-21 /pmc/articles/PMC6014444/ /pubmed/29932520 http://dx.doi.org/10.1002/mgg3.418 Text en © 2018 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. |
| spellingShingle | Corrigendum Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1 |
| title | Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1
|
| title_full | Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1
|
| title_fullStr | Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1
|
| title_full_unstemmed | Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1
|
| title_short | Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR1
|
| title_sort | whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in ryr1 |
| topic | Corrigendum |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014444/ https://www.ncbi.nlm.nih.gov/pubmed/29932520 http://dx.doi.org/10.1002/mgg3.418 |