The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions. (Q39657178)

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21 January 2020

title

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions (English)

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21 January 2020

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21 January 2020

Renate K Hukema

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21 January 2020

John Van Swieten

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21 January 2020

Yolande A L Pijnenburg

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Yolande A L Pijnenburg

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Natasja M van Schoor

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21 January 2020

Leonard H van den Berg

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Leonard H van den Berg

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Dorly J H Deeg

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21 January 2020

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Elise G P Dopper

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Petra E Cohn-Hokke

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Nayia Nicolaou

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Harro Seelaar

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J Roos A de Graaf

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Inge de Koning

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Marion Smits

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Joost Raaphorst

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21 January 2020

Helenius J Schelhaas

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21 January 2020

Christine E M De Die-Smulders

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21 January 2020

Danielle Majoor-Krakauer

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21 January 2020

Annemieke J M Rozemuller

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Rob Willemsen

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Peter Heutink

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language of work or name

English

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publication date

1 February 2012

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21 January 2020

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21 January 2020

volume

135

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21 January 2020

issue

Pt 3

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21 January 2020

page(s)

723-735

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21 January 2020

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Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement

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21 January 2018

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