Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome.
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| Title: | Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome. |
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| Authors: | Nectoux, J.1, Heron, D.2, Tallot, M.2, Chelly, J.1, Bienvenu, T.1 bienvenu@cochin.inserm.fr |
| Source: | Clinical Genetics. Jul2006, Vol. 70 Issue 1, p29-33. 5p. 1 Diagram, 1 Chart. |
| Database: | Academic Search Ultimate |
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