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contentType Journal Article|Research Support, Non-U.S. Gov't
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bibliographicCitation Issa L, Mueller K, Seufert K, Kraemer N, Rosenkotter H, Ninnemann O, Buob M, Kaindl AM, Morris-Rosendahl DJ. Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. Orphanet Journal of Rare Diseases. 2013 Apr 15;8(1):59. doi: 10.1186/1750-1172-8-59.
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date 2013-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language English
source https://pubmed.ncbi.nlm.nih.gov/
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title Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation
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Total number of triples: 41.