DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

References

Fullston T, Brueton L, Willis T. et al.
Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).

Eur J Hum Genet 2010;
18 (02) 157-162

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