CareLit · DOI-Nachweis · Aktuelle Neurologie
Autosomal dominant spastic paraplegia with sensory deficits and muscle wasting (SPG36) maps to chromosome 12q23–24
DOI 10.1055/s-2007-987537
Bibliografische Angaben
Nachweis in CareLit
Autor:innenR Schüle, A Dürr, S Forlani, J Kassubek, S Klimpe, B van de Warrenburg, L Schöls
ZeitschriftAktuelle Neurologie
Ausgabe09/2007
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Spastic paraplegias are a genetically heterogenous group of disorders. So far, over 30 genes or loci for SP have been described, among them 13 loci for autosomal dominant disease. Objective: Mapping of a novel autosomal dominant SP locus, sequencing of candidate genes and phenotypic description. Design/methods: A genome wide linkage analysis using Human Mapping 10K SNP Microarrays was performed in a larg…
Zitieren
Zitierempfehlung
R Schüle, A Dürr, S Forlani, J Kassubek, S Klimpe, B van de Warrenburg, L Schöls (2007) Autosomal dominant spastic paraplegia with sensory deficits and muscle wasting (SPG36) maps to chromosome 12q23–24. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2007-987537
Mit CareLit weiterarbeiten