Wordt geladen...
Familial Creutzfeldt-Jakob Disease in an Indian Kindred
It is now known that the inherited prion disease is caused by over 60 different mutations in the Prion protein (PRNP) gene. Four missense mutations at codons 102, 178, 200 and 210, account for over 95% of these cases. In this study we describe, a large Indian family with familial Creutzfeldt Jakob D...
Bewaard in:
| Gepubliceerd in: | Ann Indian Acad Neurol |
|---|---|
| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Wolters Kluwer - Medknow
2019
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6839320/ https://ncbi.nlm.nih.gov/pubmed/31736569 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/aian.AIAN_214_19 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|