Literature DB >> 29473684

CKAP2L mutation confirms the diagnosis of Filippi syndrome.

G Capecchi1, M Baldassarri2,3, S Ferranti1, E Guidoni1, M Cioni1, P Nürnberg4, M A Mencarelli3, A Renieri2,3, S Grosso1.   

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Year:  2018        PMID： 29473684     DOI： 10.1111/cge.13188

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  2 in total

1.  Novel variants identified in CKAP2L in two siblings with Filippi syndrome.

Authors:  Ryan J Patrick; Jill Weimer; Laura Davis-Keppen; Megan L Landsverk
Journal:  Cold Spring Harb Mol Case Stud       Date:  2022-03-24

2.  Identification of Genes Associated with the Metastasis of Pheochromocytoma/Paraganglioma Based on Weighted Gene Coexpression Network Analysis.

Authors:  Qisheng Su; Qinpei Ding; Zunni Zhang; Zheng Yang; Yuling Qiu; Xiaohong Li; Wuning Mo
Journal:  Biomed Res Int       Date:  2020-02-05       Impact factor: 3.411
  2 in total

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