Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function
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| Description | scientific article published on 19 January 2018 |
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author: Marie Coutelier Matthias Hammerschmidt Alexandra Durr Giovanni Stevanin Andrew Singleton Alexis Brice Stephan Züchner |
| Publication date | January 19, 2018 |
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