التفاصيل البيبلوغرافية
| العنوان: |
Frontotemporal lobar degeneration in Finland:molecular genetics and clinical aspects |
| المؤلفون: |
Kaivorinne, A.-L. (Anna-Lotta) |
| المساهمون: |
Remes, A. (Anne) |
| بيانات النشر: |
Oulun yliopisto, 2012. |
| سنة النشر: |
2012 |
| مصطلحات موضوعية: |
otsa-ohimolohkorappeumat, charged multi-vesicular body protein 2B, haplotype, molekyyligenetiikka, geenit, genetiikka, phenotype, repeat expansion, C9ORF72, TAR DNA binding protein, frontotemporal dementia, genotyyppi, polymorphism, geneettinen assosiaatioanalyysi, frontotemporal lobar degeneration, molecular genetics, genetics, microtubule-associated protein tau, mutation, mutaatiot, dementia |
| الوصف: |
Frontotemporal lobar degeneration (FTLD) is the second most common neurodegenerative disease leading to early-onset dementia ( |
| وصف الملف: |
application/pdf |
| اللغة: |
English |
| URL الوصول: |
https://explore.openaire.eu/search/publication?articleId=od______2423::4059be013ab06661e2d67b4ea9d8b99c
http://urn.fi/urn:isbn:9789526200132 |
| Rights: |
OPEN |
| رقم الانضمام: |
edsair.od......2423..4059be013ab06661e2d67b4ea9d8b99c |
| قاعدة البيانات: |
OpenAIRE |