✦ LIBER ✦
Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the disease
✍ Scribed by Ivan Y Iourov,Svetlana G Vorsanova,Victoria Y Voinova…
- Book ID
- 126380142
- Publisher
- BioMed Central
- Year
- 2013
- Tongue
- English
- Weight
- 499 KB
- Volume
- 6
- Category
- Article
- ISSN
- 1755-8166
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