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Alison Muir

4PUBLICATIONS
37CO-AUTHORS
Developmental genetics (incl. sex determination)NeurogeneticsNeurology and neuromuscular diseasesVirtual and mixed reality
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Journal

Publications (4)

Sort by Publication Date:
|Dec 06, 2020
FBXO28 causes developmental and epileptic encephalopathy with profound intellectual disability.

Amy L Schneider, Candace T Myers, Alison M Muir

|Oct 22, 2019
The epileptology of GNB5 encephalopathy.

Gemma Poke, Chontelle King, Alison Muir

|Oct 17, 2019
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders.

Hui Guo, Elisa Bettella, Paul C Marcogliese

|Jul 14, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.

Vincenzo Salpietro, Christine L Dixon, Hui Guo

Pageof 1

Frequent Collaborators

2 joint publications

Amy L Schneider

2 joint publications

Evan E Eichler

1 joint publications

Oscar D Bello

1 joint publications

Stephanie Efthymiou

1 joint publications

Lydie Burglen

1 joint publications

Stephanie Valence

1 joint publications

Erin Torti

1 joint publications

Andreas Lieb

1 joint publications

Conceicao Bettencourt

1 joint publications

Roope Männikkö

Frequent Collaborators

2 joint publications

Amy L Schneider

2 joint publications

Evan E Eichler

1 joint publications

Oscar D Bello

1 joint publications

Stephanie Efthymiou

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