X-linked alpha thalassemia mental retardation syndrome: Difference between revisions

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==Overview==
==Overview==
Caused by mutations in the ATR X gene. ATR X syndrome is characterised by severe learning difficulties, a characteristic facial appearance, abnormal genitalia and alpha [[thalassemia]]. The ATR protein affects the 3D structure of [[chromatin]] in the [[cell nucleus]].
Caused by mutations in the ATR X gene. ATR X syndrome is characterised by severe learning difficulties, a characteristic facial appearance, abnormal genitalia and alpha [[thalassemia]]. The ATR protein affects the 3D structure of [[chromatin]] in the [[cell nucleus]].
==References==
==References==
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[[Category:Rare diseases]]
[[Category:Rare diseases]]

Latest revision as of 17:32, 20 August 2012

X-linked alpha thalassemia mental retardation syndrome
OMIM 301040

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Overview

Caused by mutations in the ATR X gene. ATR X syndrome is characterised by severe learning difficulties, a characteristic facial appearance, abnormal genitalia and alpha thalassemia. The ATR protein affects the 3D structure of chromatin in the cell nucleus.

References


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