Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

Simple item page
dc.contributor.authorFlora Tassone
dc.contributor.authorDragana Protic
dc.contributor.authorEmily Graves Allen
dc.contributor.authorAlison D. Archibald
dc.contributor.authorAnna Baud
dc.contributor.authorTed W. Brown
dc.contributor.authorDejan B. Budimirovic
dc.contributor.authorJonathan Cohen
dc.contributor.authorBrett Dufour
dc.contributor.authorRachel Eiges
dc.contributor.authorNicola Elvassore
dc.contributor.authorLidia V. Gabis
dc.contributor.authorSamantha J. Grudzien
dc.contributor.authorDeborah A. Hall
dc.contributor.authorDavid Hessl
dc.contributor.authorAbigail Hogan
dc.contributor.authorJessica Ezzell Hunter
dc.contributor.authorPeng Jin
dc.contributor.authorPoonnada Jiraanont
dc.contributor.authorJessica Klusek
dc.contributor.authorR. Frank Kooy
dc.contributor.authorClaudine M. Kraan
dc.contributor.authorCecilia Laterza
dc.contributor.authorAndrea Lee
dc.contributor.authorKaren Lipworth
dc.contributor.authorMolly Losh
dc.contributor.authorDanuta Loesch
dc.contributor.authorReymundo Lozano
dc.contributor.authorMarsha R. Mailick
dc.contributor.authorApostolos Manolopoulos
dc.contributor.authorVeronica Martinez-Cerdeno
dc.contributor.authorYingratana McLennan
dc.contributor.authorRobert M. Miller
dc.contributor.authorFederica Alice Maria Montanaro
dc.contributor.authorMatthew W. Mosconi
dc.contributor.authorSarah Nelson Potter
dc.contributor.authorMelissa Raspa
dc.contributor.authorSusan M. Rivera
dc.contributor.authorKatharine Shelly
dc.contributor.authorPeter K. Todd
dc.contributor.authorKatarzyna Tutak
dc.contributor.authorJun Yi Wang
dc.contributor.authorAnne Wheeler
dc.contributor.authorTri Indah Winarni
dc.contributor.authorMarwa Zafarullah
dc.contributor.authorRandi J. Hagerman
dc.date.accessioned2025-07-21T06:09:56Z
dc.date.issued2023-09-21
dc.description.abstractThe premutation of the fragile X messenger ribonucleoprotein 1 (
dc.identifier.doi10.3390/cells12182330
dc.identifier.urihttps://dspace.kmitl.ac.th/handle/123456789/12821
dc.subjectFMR1
dc.subjectFragile X Syndrome
dc.subject.classificationGenetics and Neurodevelopmental Disorders
dc.titleInsight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation
dc.typeReview

Files

Collections

All