De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms

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Publication year
2018
Author(s)
Powis, Z.
Petrik, I.
Cohen, J.S.
Escolar, D.
Burton, J.
Ravenswaaij-Arts, C.M.A. van
Kleefstra, T.
Pfundt, R.P.
Tang, S.
Shinde, D.N.
Source
Clinical Genetics, 93, 5, (2018), pp. 1030-1038
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Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/191052   https://hdl.handle.net/2066/191052
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