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MECP2 mutation in male patients with non-specific X-linked mental retardation

✍ Scribed by Alfredo Orrico; Ching-Wan Lam; Lucia Galli; Maria Teresa Dotti; Giuseppe Hayek; Sui-Fan Tong; Priscilla M.K. Poon; Michele Zappella; Antonio Federico; Vincenzo Sorrentino


Book ID
117102260
Publisher
Elsevier Science
Year
2000
Tongue
English
Weight
143 KB
Volume
481
Category
Article
ISSN
0014-5793

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MECP2 gene mutations in non-syndromic X-
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## Abstract Non‐syndromic X‐linked mental retardation (MRX) is a frequent cause of inherited mental retardation. It is a heterogeneous condition in which the first 12 genes discovered to date explain no more than 15% of the MRX situations ascertained by recurrence in multiplex families. In Rett syn