A novel UBE2A mutation causes X-linked intellectual disability type Nascimento

25Citations
Citations of this article
32Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

X-linked intellectual disability (ID) type Nascimento (MIM #300860), also known as ubiquitin-conjugating enzyme E2 A (UBE2A) deficiency syndrome, is a congenital malformation syndrome characterized by moderate to severe ID, speech impairment, dysmorphic facial features, genital anomalies and skin abnormalities. Here, we report a Japanese patient with severe ID and congenital cataract. We identified a novel hemizygous mutation (c.76G>A, p.Gly26Arg) in UBE2A by whole-exome sequencing.

Cite

CITATION STYLE

APA

Tsurusaki, Y., Ohashi, I., Enomoto, Y., Naruto, T., Mitsui, J., Aida, N., & Kurosawa, K. (2017). A novel UBE2A mutation causes X-linked intellectual disability type Nascimento. Human Genome Variation, 4. https://doi.org/10.1038/hgv.2017.19

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free