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P181 Sleep myoclonus in a child with brainstem damage: a video polysomnographic study

Di Capua, M.

European journal of paediatric neurology. VOL 13; SUPP/1, ; 2009, S76 -- Elsevier Science B.V., Amsterdam Part 1; -- 2009

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De novo T362R mutation in MORC2 causes early onset cerebellar ataxia, axonal polyneuropathy and nocturnal hypoventilation

Zanni, G. et al.

European journal of paediatric neurology -- Elsevier Ltd. -- Volume: 21 S1; -- 2017

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De novo T362R mutation in MORC2 causes early onset cerebellar ataxia, axonal polyneuropathy and nocturnal hypoventilation

Zanni, G. et al.

European journal of paediatric neurology. Volume 21 (2017) Supplement 1; pp e236- -- Elsevier Ltd

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Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Travaglini, Lorena et al.

European journal of paediatric neurology -- Elsevier Ltd. -- Volume: 21 3; (pages 450-456) -- 2017

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Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Travaglini, Lorena et al.

European journal of paediatric neurology. Volume 21:Number 3 (2017, May); pp 450-456 -- Elsevier Ltd

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