Clinical features and X-inactivation in females heterozygous for creatine transporter defect.
van de Kamp JM; Mancini GM; Pouwels PJ; Betsalel OT; van Dooren SJ; de Koning I; Steenweg ME; Jakobs C; van der Knaap MS; Salomons GS; Clinical Genetics, 2011, vol. 79, issue 3, p 264, ISSN 13990004. ISBN 13990004.

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