FMR1 premutation with Prader-Willi phenotype...

Clinical Case Reports 2017 / 01

FMR1 premutation with Prader-Willi phenotype and fragile X-associated tremor/ataxia syndrome

Martínez-Cerdeño, Verónica, Lechpammer, Mirna, Noctor, Stephen, Ariza, Jeanelle, Hagerman, Paul, Hagerman, Randi
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Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.834
Date:
January, 2017
File:
PDF, 1.17 MB
english, 2017
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