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A novel deletion mutation in the ATP6V0A2 gene in an Iranian patient affected by autosomal recessive cutis laxa

Crossref DOI link: https://doi.org/10.1007/s11845-022-03246-w

Published Online: 2022-12-15

Published Print: 2023-10

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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