Rare missense TUBGCP5 gene variant in a patient with primary microcephaly

Authors

Keywords

Primary microcephaly, TUBGCP5, Tubulin gamma complex associated protein 5, Missense variant, Mild developmental delay

Journal

Volume -, Issue -, Pages -

Publisher

Elsevier BV

Online

2018-12-10

DOI

10.1016/j.ejmg.2018.12.003

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