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CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndrome

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Rademacher,  N.
Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Müller,  I.
Molecular Cytogenetics (Reinhard Ullmann), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Kalscheuer,  V. M.
Chromosome Rearrangements and Disease (Vera Kalscheuer), Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;

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Citation

Córdova-Fletes, C., Rademacher, N., Müller, I., Mundo-Ayala, J. N., Morales-Jeanhs, E. A., García-Ortiz, J. E., et al. (2010). CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndrome. Clinical Genetics, 77(1), 92-96. doi:10.1111/j.1399-0004.2009.01286.x.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-7C27-9
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