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P131 A novel CDKL5 gene mutation associated with a severe Rett syndrome-like phenotype and early onset epileptic encephalopathy

✍ Scribed by S.D. Mastroyianni; K. Voudris; E. Katsarou; A. Attilakos; D. Delis; A. Triantafillidou; A. Skardoutsou; A. Evangeliou; B. Auber; P. Burfeind

Book ID: 114359999
Publisher: Elsevier Science
Year: 2009
Tongue: English
Weight: 58 KB
Volume: 13
Category: Article
ISSN: 1090-3798
DOI: 10.1016/s1090-3798(09)70189-8

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