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- Rinaldi, C (author)
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia
- Article/chapterEnglish2015
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- American Medical Association (AMA),2015
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- LIBRIS-ID:oai:prod.swepub.kib.ki.se:131298951
- http://kipublications.ki.se/Default.aspx?queryparsed=id:131298951URI
- https://doi.org/10.1001/jamaneurol.2014.4769DOI
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- Language:English
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- Schmidt, T (author)
- Situ, AJ (author)
- Johnson, JO (author)
- Lee, PR (author)
- Chen, KL (author)
- Bott, LC (author)
- Fado, R (author)
- Harmison, GH (author)
- Parodi, S (author)
- Grunseich, C (author)
- Renvoise, B (author)
- Biesecker, LG (author)
- De Michele, G (author)
- Santorelli, FM (author)
- Filla, A (author)
- Stevanin, G (author)
- Durr, A (author)
- Brice, A (author)
- Casals, N (author)
- Traynor, BJ (author)
- Blackstone, C (author)
- Ulmer, TS (author)
- Fischbeck, KH (author)
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- In:JAMA neurology: American Medical Association (AMA)72:5, s. 561-5702168-61572168-6149
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- Bott, LC
- Fado, R
- Harmison, GH
- Parodi, S
- Grunseich, C
- Renvoise, B
- Biesecker, LG
- De Michele, G
- Santorelli, FM
- Filla, A
- Stevanin, G
- Durr, A
- Brice, A
- Casals, N
- Traynor, BJ
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