ロード中...
Molecular Genetic Diagnosis of a Bethlem Myopathy Family with an Autosomal-Dominant COL6A1 Mutation, as Evidenced by Exome Sequencing
BACKGROUND: We describe herein the application of whole exome sequencing (WES) for the molecular genetic diagnosis of a large Korean family with dominantly inherited myopathy. CASE REPORT: The affected individuals presented with slowly progressive proximal weakness and ankle contracture. They were i...
保存先:
| 出版年: | J Clin Neurol |
|---|---|
| 主要な著者: | , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Korean Neurological Association
2015
|
| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4387485/ https://ncbi.nlm.nih.gov/pubmed/25749816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3988/jcn.2015.11.2.183 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|