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1 Ergebnisse
1
SPG11mutations cause Kjellin syndrome, a hereditary spastic..:
Örlén, Hanna
;
Melberg, Atle
;
Raininko, Raili
...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 150B (2009) 7 - p. 984-992 , 2009
Link:
https://doi.org/10.1002/ajmg.b.30928
RT Journal T1 <Title>SPG11mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.b.30928&Exemplar=1&LAN=DE A1 Örlén, Hanna A1 Melberg, Atle A1 Raininko, Raili A1 Kumlien, Eva A1 Entesarian, Miriam A1 Söderberg, Per A1 Påhlman, Magnus A1 Darin, Niklas A1 Kyllerman, Mårten A1 Holmberg, Eva A1 Engler, Henry A1 Eriksson, Urban A1 Dahl, Niklas PB Wiley YR 2009 SN 1552-4841 SN 1552-485X JF American Journal of Medical Genetics Part B: Neuropsychiatric Genetics VO 150B IS 7 SP 984 OP 992 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.b.30928 DO https://doi.org/10.1002/ajmg.b.30928 SF ELIB - SuUB Bremen
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