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Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia
- Rinaldi, C (author)
- Schmidt, T (author)
- Situ, AJ (author)
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- 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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- American Medical Association (AMA), 2015
- 2015
- English.
- In: JAMA neurology. - : American Medical Association (AMA). - 2168-6157 .- 2168-6149. ; 72:5, s. 561-570
- Journal article (peer-reviewed)
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- art (subject category)
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- JAMA neurology (Search for host publication in LIBRIS)
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- By the author/editor
- Rinaldi, C
- Schmidt, T
- Situ, AJ
- Johnson, JO
- Lee, PR
- Chen, KL
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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
- Blackstone, C
- Ulmer, TS
- Fischbeck, KH
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- JAMA neurology
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- Karolinska Institutet
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