Parkin mutations and early onset parkinsonism

Brain

Volumn 126, Issue 6, 2003, Pages 1250-1251

  Morrison, Karen E ^a  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

PARKIN;

CLINICAL FEATURE; EDITORIAL; GENETIC SUSCEPTIBILITY; HUMAN; MUTATION; NEUROPATHOLOGY; NONHUMAN; PARKINSON DISEASE; PARKINSONISM; POSITRON EMISSION TOMOGRAPHY; PRIORITY JOURNAL;

AGE OF ONSET; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LIGASES; MUTATION; PARKINSONIAN DISORDERS; UBIQUITIN-PROTEIN LIGASES;

EID: 0037677644     PISSN: 00068950     EISSN: None     Source Type: Journal    
DOI: 10.1093/brain/awg189     Document Type: Editorial

References (10)

1. Abbas N, Lucking CB, Ricard S, Durr A, Bonifati V, Michele G, et al. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. Hum Mol Genet 1999; 8: 567-74.
2. Farrer M, Chan P, Chen R, Tan L, Lincoln S, Hernandez D, et al. Lewy bodies and parkinsonism in families with Parkin mutations. Ann Neurol 2001; 50: 293-300.
3. Hardy J, Cookson MR, Singleton A. Genes and parkinsonism. Lancet Neurol 2003; 2: 221-8.
4. Khan NL, Graham E, Critchley P, Schrag AE, Wood NW, Lees AJ, et al. Parkin disease: a phenotypic study of a large series of cases. Brain 2003; 126: 1279-92.
5. Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998; 392: 605-8.
6. Klein C, Pramstaller PP, Kis B, Page CC, Kann M, Leung J, et al. Parkin deletions in a family with adult-onset, tremor-dominant parkinsonism: expanding the phenotype. Ann Neurol 2000; 48: 65-71.
7. Lucking C, Durr A, Bonifiati V, Vaughan J, De Michele G, Grassor T, et al. Association between early onset Parkinson's disease and mutations in the parkin gene. New Engl J Med 2000; 342: 1560-7.
8. Periquet M, Latouche M, Lohmann E, N. Rawal, G. De Michele, S. Ricard, et al. Parkin mutations are frequent in patients with isolated early-onset parkinsonism. Brain 2003; 126: 1271-78.
9. Rawal N, Periquet M, Lohmann E, Lucking CB, Teive HA, Ambrosia G, et al. New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism. Neurology 2003; 60: 1378-81.
10. Shimura H, Hattori N, Kubo S, Mizuno Y, Asakawa S, Minishima S, et al. Familial Parkinson's disease gene product, parkin, is a ubiquitin-protein ligase. Nature Genet 2000; 25: 302-5.