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Paper Details

Reversal of neurobehavioral social deficits in dystrophic mice using inhibitors of phosphodiesterases PDE5A and PDE9A.
Transl Psychiatry
11
2016
DYSTROPHIN gene, Duchenne muscular dystrophy, PDE5A, PDE9A, PDE9A enzymes, autism spectrum disorder, cGMP, cGMP-specific PDE5A, cerebellar deficits, dystrophic, dystrophin, mice, muscle wasting, patients, phosphodiesterases
Author NameAffiliation
Jamie L MarshallBoston Children's Hospital
Michael J FeyderBoston Children's Hospital
Mustafa SahinBoston Children's Hospital, Harvard Medical School
Louis M KunkelBoston Children's Hospital
Louis M KunkelHarvard Medical School
Louis M KunkelBoston Children's Hospital
Louis M KunkelThe Manton Center for Orphan Diseases
Louis M KunkelHarvard Stem Cell Institute
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