Maternal uniparental heterodisomy with partial isodisomy of a chromosome 2 carrying a splice acceptor site mutation (IVS9-2A>T) in ALS2 causes infantile-onset ascending spastic paralysis (IAHSP)

Author： Herzfeld Thilo  

Publisher： Springer Publishing Company

ISSN： 1364-6745

Source： Neurogenetics, Vol.10, Iss.1, 2009-02, pp. : 59-64

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