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Identification of a novelCDKL5exon and pathogenic mutations in patients with severe mental retardation, early-onset seizures and Rett-like features

✍ Scribed by Nils Rademacher; Melanie Hambrock; Ute Fischer; Bettina Moser; Berten Ceulemans; Wolfgang Lieb; Rainer Boor; Irina Stefanova; Gabriele Gillessen-Kaesbach; Charlotte Runge; Georg Christoph Korenke; Stefanie Spranger; Franco Laccone; Andreas Tzschach; Vera M. Kalscheuer


Publisher
Springer
Year
2011
Tongue
English
Weight
169 KB
Volume
12
Category
Article
ISSN
1364-6745

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