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Search: WFRF:(Sanotsky Y) > Opala G > Strongosky A J > DNAJC13 p.Asn855Ser...

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DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

Lorenzo-Betancor, O (author)
Ogaki, K (author)
Soto-Ortolaza, A I (author)
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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, Andreas (author)
Lund 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
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)
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 (creator_code:org_t)
2015-08-17
2015
English.
In: European Journal of Neurology. - : Wiley. - 1351-5101. ; 22:9, s. 1323-1325
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

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