Cite
HARVARD Citation
Han, E. et al. (2020). A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations. Ophthalmic genetics. pp. 363-367. [Online].
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Han, E. et al. (2020). A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations. Ophthalmic genetics. pp. 363-367. [Online].