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- Lorenzo-Betancor, O (author)
DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.
- Article/chapterEnglish2015
Publisher, publication year, extent ...
- 2015-08-17
- Wiley,2015
Numbers
- LIBRIS-ID:oai:lup.lub.lu.se:844255bd-def6-46a8-8f0f-c0aa8a6e80b6
- https://lup.lub.lu.se/record/7840808URI
- https://doi.org/10.1111/ene.12770DOI
Supplementary language notes
- Language:English
- Summary in:English
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Notes
- Recently, a novel mutation in exon 24 of DNAJC13 gene (p.Asn855Ser, rs387907571) has been reported to cause autosomal dominant Parkinson's disease (PD) in a multi-incident Mennonite family.
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Added entries (persons, corporate bodies, meetings, titles ...)
- Ogaki, K (author)
- Soto-Ortolaza, A I (author)
- Labbe, C (author)
- Walton, R L (author)
- Strongosky, A J (author)
- van Gerpen, J A (author)
- Uitti, R J (author)
- McLean, P J (author)
- Springer, W (author)
- Siuda, J (author)
- Opala, G (author)
- Krygowska-Wajs, A (author)
- Barcikowska, M (author)
- Czyzewski, K (author)
- McCarthy, A (author)
- Lynch, T (author)
- Puschmann, AndreasLund University,Lunds universitet,Neurologi, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Neurology, Lund,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine(Swepub:lu)med-aps (author)
- Rektorova, I (author)
- Sanotsky, Y (author)
- Vilariño-Güell, C (author)
- Farrer, M J (author)
- Ferman, T J (author)
- Boeve, B F (author)
- Petersen, R C (author)
- Parisi, J E (author)
- Graff-Radford, N R (author)
- Dickson, D W (author)
- Wszolek, Z K (author)
- Ross, O A (author)
- Neurologi, LundSektion IV (creator_code:org_t)
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- In:European Journal of Neurology: Wiley22:9, s. 1323-13251351-5101
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