Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly (Q41929246)

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scientific article published on 16 October 2014
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Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly
scientific article published on 16 October 2014

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    Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly (English)

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