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

doi:10.1111/j.1399-0004.2010.01460.x

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 journal › Article › Academic › peer-review

Original language	Undefined/Unknown
Pages (from-to)	264-272
Journal	Clinical Genetics
Volume	79
Issue number	3
DOIs	https://doi.org/10.1111/j.1399-0004.2010.01460.x
Publication status	Published - 2011

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10.1111/j.1399-0004.2010.01460.x

Cite this

van de Kamp, J. M., Mancini, G. M. S., Pouwels, P. J. W., Betsalel, O. T., van Dooren, S. J. M., de Koning, I., ... Salomons, G. S. (2011). Clinical features and X-inactivation in females heterozygous for creatine transporter defect. Clinical Genetics, 79(3), 264-272. https://doi.org/10.1111/j.1399-0004.2010.01460.x

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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.A.J.M.; van der Knaap, M.S.; Salomons, G.S.

In: Clinical Genetics, Vol. 79, No. 3, 2011, p. 264-272.

Research output: Contribution to journal › Article › Academic › peer-review

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T1 - Clinical features and X-inactivation in females heterozygous for creatine transporter defect

AU - van de Kamp, J.M.

AU - Mancini, G.M.S.

AU - Pouwels, P.J.W.

AU - Betsalel, O.T.

AU - van Dooren, S.J.M.

AU - de Koning, I.

AU - Steenweg, M.E.

AU - Jakobs, C.A.J.M.

AU - van der Knaap, M.S.

AU - Salomons, G.S.

PY - 2011

Y1 - 2011

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DO - 10.1111/j.1399-0004.2010.01460.x

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JO - Clinical Genetics

JF - Clinical Genetics

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