Amanote Research

Amanote Research

    RegisterSign In

Xp11.22 Deletions Encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a Cause of Syndromic X-Linked Intellectual Disability

PLoS ONE - United States
doi 10.1371/journal.pone.0175962
Full Text
Open PDF
Abstract

Available in full text

Categories
Multidisciplinary
Date

April 17, 2017

Authors
Christina GrauMolly StarkovichMahshid S. AzamianFan XiaSau Wai CheungPatricia EvansAlex HendersonSeema R. LalaniDaryl A. Scott
Publisher

Public Library of Science (PLoS)


Related search

Exons Deletion of CNKSR2 Gene Identified in X-Linked Syndromic Intellectual Disability

BMC Medical Genetics
Genetics
2020English

Subtle Functional Defects in the Arf-Specific Guanine Nucleotide Exchange Factor IQSEC2 Cause Non-Syndromic X-Linked Intellectual Disability

Small GTPases
BiochemistryCell Biology
2010English

X-Linked Intellectual Disability, Cantagrel Type

2020English

X-Linked Intellectual Disability, Pai Type

2020English

X-Linked Intellectual Disability, Stoll Type

2020English

X-Linked Intellectual Disability, Schimke Type

2020English

X-Linked Intellectual Disability, Najm Type

2020English

X-Linked Intellectual Disability-Acromegaly-Hyperactivity Syndrome

2020English

X-Linked Intellectual Disability-Retinitis Pigmentosa Syndrome

2020English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2026 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy