Clinical and genetic characterization of a cohort of 97 CLN6 patients tested at a single center.
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Orphanet J Rare Dis. 2022 May 3;17(1):179. doi: 10.1186/s13023-022-02288-8.
Orphanet J Rare Dis. 2022.
PMID: 35505348
Free PMC article.