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Study links Fragile X Syndrome proteins and RNA editing mistakes at nerve-muscle junction
10:00 EDT 30 Oct 2011 | Physorg.COM
The most common form of heritable cognitive impairment is Fragile X Syndrome, caused by mutation or malfunction of the FMR1 gene. Loss of FMR1 function is also the most common genetic cause of autism. Understanding how this gene works is vital to fin..
Original Article: Study links Fragile X Syndrome proteins and RNA editing mistakes at nerve-muscle junction
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Fragile X?Associated Tremor Ataxia Syndrome FXTAS
Proteins
Third Cranial Nerve Disorders
Optic Nerve Disorders
Vagus nerve stimulation
Nerve Root Disorders
Interdigital Nerve Pain
Nerve Compression Syndromes
Optic nerve appearance
Fourth Cranial Nerve Palsy
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