ロード中...
Two novel mutations of FBN1 in Jordanian patients with Marfan syndrome
Marfan syndrome is an autosomal dominant inheritance disorder with a 1/5000-live-birth prevalence. More than 3000 mutations have been characterized thus far in the FBN1 gene. The goal of this study is to facilitate Marfan syndrome diagnosis in Jordanian patients using a molecular genetic testing. Al...
保存先:
| 出版年: | Int J Clin Exp Med |
|---|---|
| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
e-Century Publishing Corporation
2015
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4694396/ https://ncbi.nlm.nih.gov/pubmed/26770496 |
| 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!
|