Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome.

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Bibliographic Details
Title: Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome.
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
Description
ISSN:00099163
DOI:10.1111/j.1399-0004.2006.00629.x