A novel homozygous missense variant in POC1B causes cone dystrophy in a consanguineous Pakistani family
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Authors
Asad Munir
Asad Munir•Inam Khan•Atta Rehman
Published
November 20, 2024
Abstract
Background Cone dystrophy is a heterogeneous hereditary retinal disorder with disease symptoms appearing in the late first or early second decades of life.
