Mutación de novo en DYNC1H1, atrofia muscular espinal y problemas atencionales / DYNC1H1 de novo mutation, spinal muscular atrophy and attention problems
Neurología (Barc., Ed. impr.)
; 37(5): 406-409, Jun. 2022. ilus
Article
in English, Spanish
| IBECS
| ID: ibc-205991
Responsible library:
ES1.1
Localization: ES15.1 - BNCS
Fulltext
- https://www.sciencedirect.com/science/article/pii/S0213485321001262
- https://pdf.sciencedirectassets.com/280280/1-s2.0-S0213485321X00060/1-s2.0-S0213485321001262/main.pdf?X-Amz-Security-Token=IQoJb3JpZ2luX2VjELX%2F%2F%2F%2F%2F%2F%2F%2F%2F%2FwEaCXVzLWVhc3QtMSJGMEQCICFVBKk49bQSULP9ldyIrPLKuSZ1tVUhw%2BlCVCtYJXMqAiBlpRmpsZm7Sc9JcuDoAayv%2FXGoByeBZR6izUSlxTg4kirbBAju%2F%2F%2F%2F%2F%2F%2F%2F%2F%2F8BEAQaDDA1OTAwMzU0Njg2NSIMqpdT8yNg6A%2BoT%2FAtKq8ELwjc%2Bm1nCPE8T95cbuemEVZtbYxuOBhkV0fYiznitUYuSYnWOEVu6%2BK2F4D6OTTEcobrba2iVgU02mqN64oT%2BeIbcdvmDQshoH601A0EZ9iXDFKxJxPAg0KIto6cjzXobbmoQhylMCmR7WdENVHD1rz7MO1AbKZLLZGX01RVpII2h7dCCg6djDhgLM1zyDBlGE1ie4riybRAi9CNzTbQtIM3TGU7dYk1JzTQ42I0KhY2fTuev65vkl0rL8GcrtjJVdFp2MjfcTe0ZA6CZtaU9T%2F5qamBDI1jXFZ5p%2FYaU9UFPIYZob6Kf1RdRAzMpxk0f8lrUa4dl9c5oThHRJiiLr2WFRf7%2B%2Byz1OZQmoxs8X5u4FmEKWVbhqdQUe4hmv6LEd9QFhJVaM4gXMDsuKp4nhhGq4swIa9joTFLieGSjX8yDXIKWer30ZHaldv6PlL6ciqIagC1F2fByNoZkv0oDOcNdqbxajdT4xeYzFfE%2B1lrCHD5rTr6d5sWhFZioNTOATVWnvbRvB27Z1pv10MZmgUUIEcU%2FoJwMb0WuN6%2BE64FrAwLCBf65%2BrAtuAtCugTY5tF%2BSEds4xp0nGXoSEVU9b1mf4n8bfjVG31OsZKFrrvSFNQQKwVRv0yROc0%2F8MVElBTQCsLNRfoJjRGKNVLwAbkwUCVk3mVFdmewObYIWGfwTbua3WfwhTwGRmr4QbMcBTWQDeKaXqgY9LnMm8fa8bKxwk0itnuu2ZGF7biZjCPqtWWBjqqAcx6qrnuN8yC%2FMjtKYZTO4hli7SmqY4yD%2BtgwOrlr%2BMHJc4thDmUIel7HXy%2BU7vCLQQKRg33D%2Bdd66FIUCOF2s0BEbSg%2BaABTBJyR0NFXr6dNOnbUlWLIBjt2LIhCe6FHgS9Oo26cJ2c18iIj30VjQwRRBTsMAdCi77hSYFFDOpDpY69mlkC9mcWFOZcrUjM%2FP1AhIb4dSTuRB2Bzw84HL0OjAuvoKDEX1Xm&X-Amz-Algorithm=AWS4-HMAC-SHA256&X-Amz-Date=20220718T132647Z&X-Amz-SignedHeaders=host&X-Amz-Expires=300&X-Amz-Credential=ASIAQ3PHCVTY7PGVN6XK%2F20220718%2Fus-east-1%2Fs3%2Faws4_request&X-Amz-Signature=bfb56465c97780dc922fd8f1dba577cdcd2ab2e75d3de5e0a528cc4d88c9df84&hash=f9dfbc62a7e1662f4e19e7597f403dda29c9d122af6ac5b006bd5bb2f3c27ccd&host=68042c943591013ac2b2430a89b270f6af2c76d8dfd086a07176afe7c76c2c61&pii=S0213485321001262&tid=spdf-045daa4b-5290-488e-a73c-e8190624aa31&sid=e1d5b0896b5ad340d86871a6d8411685f3bagxrqa&type=client&ua=4d5c04005d07560a0b5a&rr=72cb8d0ed9ea08c0
- https://reader.elsevier.com/reader/sd/pii/S2173580822000347?token=16ACDC55DD2EBE8842A8B7364C0FC42B76DE15B2BBA9DC204EDD217F1F10C79D17628EA656C35FFEBFD17887F5A369D1&originRegion=us-east-1&originCreation=20220718133832
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Muscular Atrophy, Spinal
/
Charcot-Marie-Tooth Disease
Limits:
Humans
Language:
English
/
Spanish
Journal:
Neurología (Barc., Ed. impr.)
Year:
2022
Document type:
Article
Institution/Affiliation country:
Hospital Universitario Quirónsalud/España
/
NIMGenetics/España