A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Hanadi A. Abdelrahman; Aisha M. Al-Shamsi; Bassam R. Ali; Lihadh Al-Gazali

doi:10.1111/cge.13443

A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

Hanadi A. Abdelrahman
, Aisha M. Al-Shamsi
, Bassam R. Ali
, Lihadh Al-Gazali

Research output: Contribution to journal › Letter › peer-review

Original language	English
Pages (from-to)	586-587
Number of pages	2
Journal	Clinical Genetics
Volume	94
Issue number	6
DOIs	https://doi.org/10.1111/cge.13443
Publication status	Published - Dec 2018

ASJC Scopus subject areas

Genetics
Genetics(clinical)

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10.1111/cge.13443

Cite this

@article{776f1b4dc30043579bf38d93d74ff403,

title = "A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease",

author = "Abdelrahman, \{Hanadi A.\} and Al-Shamsi, \{Aisha M.\} and Ali, \{Bassam R.\} and Lihadh Al-Gazali",

note = "Funding Information: The project was funded by UAE University grants (31 M241 \& 31R126) and approved by Al-Ain Medical-Human-Research-Ethics-Committee according to national regulations (10/09, ERH 2015-3241 15-115).",

year = "2018",

month = dec,

doi = "10.1111/cge.13443",

language = "English",

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T1 - A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

AU - Abdelrahman, Hanadi A.

AU - Al-Shamsi, Aisha M.

AU - Ali, Bassam R.

AU - Al-Gazali, Lihadh

N1 - Funding Information: The project was funded by UAE University grants (31 M241 & 31R126) and approved by Al-Ain Medical-Human-Research-Ethics-Committee according to national regulations (10/09, ERH 2015-3241 15-115).

PY - 2018/12

Y1 - 2018/12

UR - https://www.scopus.com/pages/publications/85054748482

UR - https://www.scopus.com/pages/publications/85054748482#tab=citedBy

U2 - 10.1111/cge.13443

DO - 10.1111/cge.13443

M3 - Letter

C2 - 30308082

AN - SCOPUS:85054748482

SN - 0009-9163

VL - 94

SP - 586

EP - 587

JO - Clinical Genetics

JF - Clinical Genetics

IS - 6

ER -

A null variant in PUS3 confirms its involvement in intellectual disability and further delineates the associated neurodevelopmental disease

ASJC Scopus subject areas

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