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Literature summary for 2.7.11.22 extracted from
- Clinical and cellular features in patients with primary autosomal recessive microcephaly and a novel CDK5RAP2 mutation. (2013), Orphanet J Rare Dis, 8, 59.
Organism
| Organism | UniProt | Comment | Textmining |
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Release 2023.1 (January 2023)
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