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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.
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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  Data: Maternal origin of a novel C-terminal truncation mutation in CDKL5 causing a severe atypical form of Rett syndrome.
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  Data: <searchLink fieldCode="AR" term="%22Nectoux%2C+J%2E%22">Nectoux, J.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Heron%2C+D%2E%22">Heron, D.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Tallot%2C+M%2E%22">Tallot, M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Chelly%2C+J%2E%22">Chelly, J.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Bienvenu%2C+T%2E%22">Bienvenu, T.</searchLink><relatesTo>1</relatesTo><i> bienvenu@cochin.inserm.fr</i>
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  Data: <searchLink fieldCode="JN" term="%22Clinical+Genetics%22">Clinical Genetics</searchLink>. Jul2006, Vol. 70 Issue 1, p29-33. 5p. 1 Diagram, 1 Chart.
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        Value: 10.1111/j.1399-0004.2006.00629.x
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              Text: Jul2006
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