CareLit · DOI-Nachweis · Klinische Neurophysiologie
The P56S mutation in the VAPB gene is not due to a single founder
DOI 10.1055/s-2008-1072959
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Nachweis in CareLit
Autor:innenA Funke
ZeitschriftKlinische Neurophysiologie
Ausgabe04/2008
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: The P56S mutation in the vesicle associated membrane protein associated protein B (VAPB) gene has been described in Brazilian families of Portuguese origin showing different phenotypes of motor neuron disorders including ALS and spinal muscular atrophy. The mutation was due to a common founder in the Brazilian families and has not been described in European populations so far. Methods: We analysed eleven…
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Zitierempfehlung
A Funke (2008) The P56S mutation in the VAPB gene is not due to a single founder. Klinische Neurophysiologie (04). https://doi.org/10.1055/s-2008-1072959
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