Cite
HARVARD Citation
Bryant, L. et al. (2018). On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness. Ophthalmic genetics. pp. 144-146. [Online].
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Bryant, L. et al. (2018). On variants and disease-causing mutations: Case studies of a SEMA4A variant identified in inherited blindness. Ophthalmic genetics. pp. 144-146. [Online].