Clinical features and X-inactivation in females heterozygous for creatine transporter defect.
van de Kamp, J. M.; Mancini, G. M. S.; Pouwels, P. J. W.; Betsalel, O. T.; van Dooren, S. J. M.; de Koning, I.; Steenweg, M. E.; Jakobs, C.; van der Knaap, M. S.; Salomons, G. S.; Clinical Genetics, 2011, vol. 79, issue 3, p 264, ISSN 00099163. ISBN 13990004.

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