RSK2 mutation co-segregates with X-linked...

Clinical Genetics 2014 / 01 Vol. 85; Iss. 1

RSK2 mutation co-segregates with X-linked intellectual disability and attenuated Coffin-Lowry phenotype in a three-generation family

Maystadt, I, Destree, A, Benoit, V, Aeby, A, Lederer, D, Moortgat, S, Jurkiewicz, D, Krajewska-Walasek, M, Hanauer, A, Thomas, GM
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Volume:
85
Language:
english
Journal:
Clinical Genetics
DOI:
10.1111/cge.12122
Date:
January, 2014
File:
PDF, 653 KB
english, 2014
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