Voice of People with Fragile X Syndrome and Their Families: Reports from a Survey on Treatment Priorities

To date, there has been limited research on the primary concerns and treatment priorities for individuals with fragile X syndrome (FXS) and their families. The National Fragile X Foundation in collaboration with clinical investigators from industry and academia constructed a survey to investigate th...

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Veröffentlicht in:Brain sciences Jg. 9; H. 2; S. 18
Hauptverfasser: Weber, Jayne Dixon, Smith, Elizabeth, Berry-Kravis, Elizabeth, Cadavid, Diego, Hessl, David, Erickson, Craig
Format: Journal Article
Sprache:Englisch
Veröffentlicht: Switzerland MDPI AG 23.01.2019
MDPI
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ISSN:2076-3425, 2076-3425
Online-Zugang:Volltext
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