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== | ||
{{reflist|2}} | {{reflist|2}} | ||
{{SIB}} | |||
[[Category:Rare diseases]] | [[Category:Rare diseases]] |
Revision as of 14:32, 23 July 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.