Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Wilhelm Schaible"'
Autor:
Liang Tong, Ludger Schöls, Robert Hering, Christine Klein, Daniela Berg, Bernd Wollnik, Dirk Woitalla, Eva-Maria Mietz, Jörg B. Schulz, Rejko Krüger, Wilhelm Schaible, Xiao Tao, Karsten M. Strauss, Olaf Riess, Peter Bauer, Thomas Müller, Andreas Bauer, Slobodanka Petrovic, Philipp T. Meyer
Publikováno v:
Human Mutation. 24:321-329
Mutations in the parkin gene have been identified as a common cause of autosomal recessive inherited Parkinson disease (PD) associated with early disease manifestation. However, based on linkage data, mutations in other genes contribute to the geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1114f8fc0dcce1e2c45e0a770e29e8a9
https://doi.org/10.1002/humu.20089
https://doi.org/10.1002/humu.20089
Autor:
Robert, Hering, Karsten M, Strauss, Xiao, Tao, Andreas, Bauer, Dirk, Woitalla, Eva-Maria, Mietz, Slobodanka, Petrovic, Peter, Bauer, Wilhelm, Schaible, Thomas, Müller, Ludger, Schöls, Christine, Klein, Daniela, Berg, Philipp T, Meyer, Jörg B, Schulz, Bernd, Wollnik, Liang, Tong, Rejko, Krüger, Olaf, Riess
Publikováno v:
Human mutation. 24(4)
Mutations in the parkin gene have been identified as a common cause of autosomal recessive inherited Parkinson disease (PD) associated with early disease manifestation. However, based on linkage data, mutations in other genes contribute to the geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d2efbaa38f10d934c5a214db2b21dd4
https://pubmed.ncbi.nlm.nih.gov/15365989
https://pubmed.ncbi.nlm.nih.gov/15365989