Lataa...
Improved method for molecular diagnosis of myotonic dystrophy type 1 (DM1)
Myotonic dystrophy type 1 (DM1) has been identified as the amplification of a polymorphic (CTG)n repeat in the 3′ untranslated region of a gene encoding a serine/threonine kinase (DMPK). The length of the CTG repeat correlates with clinical severity and the age at onset of the disease. Thus, the abi...
Tallennettuna:
| Julkaisussa: | J Clin Lab Anal |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Wiley Subscription Services, Inc., A Wiley Company
2004
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807958/ https://ncbi.nlm.nih.gov/pubmed/14730559 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.20004 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|