Rescue of fragile X syndrome phenotypes inFmr1KO mice by a...

Orphanet Journal of Rare Diseases 2014 / 12 Vol. 9; Iss. 1

Rescue of fragile X syndrome phenotypes inFmr1KO mice by a BKCa channel opener molecule

Betty Hébert,Susanna Pietropaolo,Sandra Même…
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Volume:
9
Language:
english
Journal:
Orphanet Journal of Rare Diseases
DOI:
10.1186/s13023-014-0124-6
Date:
December, 2014
File:
PDF, 1.04 MB
english, 2014
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