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Maystadt, I. et al. (n.d.). RSK2 mutation co‐segregates with X‐linked intellectual disability and attenuated Coffin–Lowry phenotype in a three‐generation family. Clinical genetics. pp. 96-99. [Online].
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Maystadt, I. et al. (n.d.). RSK2 mutation co‐segregates with X‐linked intellectual disability and attenuated Coffin–Lowry phenotype in a three‐generation family. Clinical genetics. pp. 96-99. [Online].