Nature Genetics
37, 1044 - 1046 (2005)
Published online: 25 September 2005; | doi:10.1038/ng1649
Mutations in SEPT9 cause hereditary neuralgic amyotrophyGregor Kuhlenbäumer, Mark C Hannibal, Eva Nelis, Anja Schirmacher, Nathalie Verpoorten, Jan Meuleman, Giles D J Watts, Els De Vriendt, Peter Young, Florian Stögbauer, Hartmut Halfter, Joy Irobi, Dirk Goossens, Jurgen Del-Favero, Benjamin G Betz, Hyun Hor, Gert Kurlemann, Thomas D Bird, Eila Airaksinen, Tarja Mononen, Adolfo Pou Serradell, José M Prats, Christine Van Broeckhoven, Peter De Jonghe, Vincent Timmerman, E Bernd Ringelstein
& Phillip F Chance Supplementary Fig. 1 (pdf 20K)
Recombination events in HNA families used to narrow down the candidate region. Supplementary Fig. 2 (pdf 40K)
Allele sharing between HNA-families and informative recombinants in family K4018. Supplementary Table 1 (pdf 20K)
Self-generated STR-markers. Supplementary Table 2 (pdf 16K)
Primers and PCR-conditions for the mutations analysis of SEPT9 on genomic DNA. Supplementary Table 3 (pdf 16K)
PCR-primers, conditions and restriction enzymes for the PCR-RFLP analysis of SEPT9 mutations. Supplementary Table 4 (pdf 16K)
Accession numbers of SEPT9 cDNAs.
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