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Refined mapping of X-linked reticulate pigmentary disorder and sequencing of candidate genes.
Hum Genet. 2008 Jun;123(5):469-76. doi: 10.1007/s00439-008-0498-4. Epub 2008 Apr 11.
Hum Genet. 2008.
PMID: 18404279
Free PMC article.
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardation.
Field M, Tarpey P, Boyle J, Edkins S, Goodship J, Luo Y, Moon J, Teague J, Stratton MR, Futreal PA, Wooster R, Raymond FL, Turner G.
Field M, et al.
Clin Genet. 2006 Dec;70(6):509-15. doi: 10.1111/j.1399-0004.2006.00723.x.
Clin Genet. 2006.
PMID: 17100996
Free PMC article.
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