Clinical features and X-inactivation in females heterozygous for creatine transporter defect

J.M. van de Kamp, G.M.S. Mancini, P.J.W. Pouwels, O.T. Betsalel, S.J.M. van Dooren, I. de Koning, M.E. Steenweg, C.A.J.M. Jakobs, M.S. van der Knaap, G.S. Salomons

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)264-272
JournalClinical Genetics
Issue number3
Publication statusPublished - 2011

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