IndraLab

Statements


Mutated CACNA1F activates CSNB2. 1 / 1
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reach
"However, there are a few reports of atypical cases of vision loss progressing alongside the appearance of retinal and optic disc atrophy in patients with CSNB2 caused by CACNAF1 mutations [XREF_BIBR, XREF_BIBR]."