A novel fragile X syndrome mutation reveals a conserved role for the carboxy‐terminus in FMRP localization and function-Reference-Cited by-同舟云学术

A novel fragile X syndrome mutation reveals a conserved role for the carboxy‐terminus in FMRP localization and function

Published:2015-02-18 Issue:4 Volume:7 Page:423-437
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Okray Zeynep¹²³,Esch Celine EF⁴,Van Esch Hilde²,Devriendt Koen²,Claeys Annelies¹²,Yan Jiekun¹²,Verbeeck Jelle¹²,Froyen Guy¹²,Willemsen Rob⁴,Vrij Femke MS⁵,Hassan Bassem A¹²³

Affiliation:

1. VIB Center for the Biology of Disease VIB Leuven Belgium

2. Center for Human Genetics University of Leuven School of Medicine and University Hospitals Leuven Leuven Belgium

3. Program in Molecular and Developmental Genetics Doctoral School of Biomedical Sciences University of Leuven Leuven Belgium

4. Department of Clinical Genetics Erasmus Medical Center Rotterdam The Netherlands

5. Department of Psychiatry Erasmus Medical Center Rotterdam The Netherlands

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201404576

Reference62 articles.

1. Axonal Injury and Regeneration in the Adult Brain of Drosophila

2. From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome

3. Immunocytochemical and Biochemical Characterization of FMRP, FXR1P, and FXR2P in the Mouse

4. Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function

5. Conversational Characteristics of Children With Fragile X Syndrome: Repetitive Speech

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