Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease
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| Description | scientific article published on 27 November 2013 |
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author: Svetlana G. Vorsanova Victoria Y Voinova Yuri B. Yurov Maria A. Zelenova |
| Publication date | November 27, 2013 |
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