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Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation.

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Bibliographic Details
Title: Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation.
Authors: Issa, Lina1,2, Mueller, Katrin3, Seufert, Katja3, Kraemer, Nadine1,2, Rosenkotter, Henning4, Ninnemann, Olaf1, Buob, Michael4, Kaindl, Angela M.1,2 angela.kaindl@charite.de, Morris-Rosendahl, Deborah J.3,5 deborah.morris-rosendahl@uniklinik-freiburg.de
Source: Orphanet Journal of Rare Diseases. 2013, Vol. 8 Issue 1, Special section p1-14. 14p. 5 Color Photographs, 2 Black and White Photographs, 1 Chart.
Database: Academic Search Ultimate
Description
ISSN:17501172
DOI:10.1186/1750-1172-8-59