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Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia

✍ Scribed by Zoran Brkanac; Nicola H. Chapman; Mark M. Matsushita; Lani Chun; Kathleen Nielsen; Elizabeth Cochrane; Virginia W. Berninger; Ellen M. Wijsman; Wendy H. Raskind


Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
71 KB
Volume
144B
Category
Article
ISSN
1552-4841

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Evaluation of two X chromosomal candidat
✍ Wan, Minghong; Francke, Uta πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 24 KB

The most likely cause of the Rett syndrome (RTT) is an X-linked dominant mutation lethal in hemizygous males. Previous exclusion mapping studies have identified putative regions for the RTT gene on the X chromosome. In the present study, we evaluated two candidate genes, glutamate dehydrogenase-2 (G