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Comment

. 2005 Apr;365(9466):1229-30.

doi: 10.1016/S0140-6736(05)74809-1.

LRRK2 mutations and Parkinsonism

Mathias Toft, Ignacio F Mata, Jennifer M Kachergus, Owen A Ross, Matthew J Farrer

PMID: 15811454
DOI: 10.1016/S0140-6736(05)74809-1

Comment

LRRK2 mutations and Parkinsonism

Mathias Toft et al. Lancet. 2005 Apr.

. 2005 Apr;365(9466):1229-30.

doi: 10.1016/S0140-6736(05)74809-1.

Authors

Mathias Toft, Ignacio F Mata, Jennifer M Kachergus, Owen A Ross, Matthew J Farrer

PMID: 15811454
DOI: 10.1016/S0140-6736(05)74809-1

No abstract available

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Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
Nichols WC, Pankratz N, Hernandez D, Paisán-Ruíz C, Jain S, Halter CA, Michaels VE, Reed T, Rudolph A, Shults CW, Singleton A, Foroud T; Parkinson Study Group-PROGENI investigators. Nichols WC, et al. Lancet. 2005 Jan 29-Feb 4;365(9457):410-2. doi: 10.1016/S0140-6736(05)17828-3. Lancet. 2005. PMID: 15680455
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.
Di Fonzo A, Rohé CF, Ferreira J, Chien HF, Vacca L, Stocchi F, Guedes L, Fabrizio E, Manfredi M, Vanacore N, Goldwurm S, Breedveld G, Sampaio C, Meco G, Barbosa E, Oostra BA, Bonifati V; Italian Parkinson Genetics Network. Di Fonzo A, et al. Lancet. 2005 Jan 29-Feb 4;365(9457):412-5. doi: 10.1016/S0140-6736(05)17829-5. Lancet. 2005. PMID: 15680456
A common LRRK2 mutation in idiopathic Parkinson's disease.
Gilks WP, Abou-Sleiman PM, Gandhi S, Jain S, Singleton A, Lees AJ, Shaw K, Bhatia KP, Bonifati V, Quinn NP, Lynch J, Healy DG, Holton JL, Revesz T, Wood NW. Gilks WP, et al. Lancet. 2005 Jan 29-Feb 4;365(9457):415-6. doi: 10.1016/S0140-6736(05)17830-1. Lancet. 2005. PMID: 15680457

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