Biallelicframeshift mutation in RIN2 in a patient with intellectual disability and cataract, without RIN2 syndrome

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Publication year
2017
Author(s)
Amen-Hellebrekers, C.J. van
Jansen, S
Stegmann, A.P.
Stevens, S.J.
Pfundt, R.P.
Vries, B.B.A. de
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American Journal of Medical Genetics. Part A, 173, 12, (2017), pp. 3238-3240
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Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/179551   https://hdl.handle.net/2066/179551
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