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New Parkin Mutations and Atypical Phenotypes in Families with Autosomal Recessive Parkinsonism
AuthID
P-000-H1E
P-000-H1E
21
Author(s)
Rawal, N
·Periquet, M
·Lohmann, E
·Lucking, CB
·Teive, HA
·Ambrosio, G
·Raskin, S
·Lincoln, S
·Hattori, N
·Guimaraes, J
·[+1]·
Bele, WD
·Destee, A
·Mizuno, Y
·Farrer, M
·Deleuze, JF
·De Michele, G
·Agid, Y
·Durr, A
·Brice, A
2
Group Author(s)
French Parkinsons's Dis Genetics S; European Consortium Genetic Sus
Publication Identifiers
Pubmed: 12707451
Scopus: 2-s2.0-0037461335
Wos: WOS:000182489600035
Source Identifiers
ISSN: 0028-3878
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| Name Order | Name | Name Order | Name | Name Order | Name | ||
|---|---|---|---|---|---|---|---|
| 1 | Rawal, N; | 2 | Periquet, M; | 3 | Lohmann, E; | ||
| 4 | Lucking, CB; | 5 | Teive, HA; | 6 | Ambrosio, G; | ||
| 7 | Raskin, S; | 8 | Lincoln, S; | 9 | Hattori, N; | ||
| 10 | Guimaraes, J; | 11 | Horstink, MWIM; | 12 | Bele, WD; | ||
| 13 | Brousolle, E; | 14 | Destee, A; | 15 | Mizuno, Y; | ||
| 16 | Farrer, M; | 17 | Deleuze, JF; | 18 | De Michele, G; | ||
| 19 | Agid, Y; | 20 | Durr, A; | 21 | Brice, A; |
