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Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability

Crossref DOI link: https://doi.org/10.1038/s10038-025-01422-1

Published Online: 2025-11-10

Published Print: 2026-01

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

Authors

Inoue, Yuta https://orcid.org/0000-0002-7073-2843
Tsuchida, Naomi https://orcid.org/0000-0001-7203-884X
Kim, Chong Ae https://orcid.org/0000-0002-1754-1300
de Oliveira Stephan, Bruno

Castro, Matheus Augusto Araujo https://orcid.org/0000-0003-0335-8799
Honjo, Rachel Sayuri

Bertola, Debora Romeo

Uchiyama, Yuri https://orcid.org/0000-0002-4540-5277
Hamanaka, Kohei

Fujita, Atsushi

Koshimizu, Eriko https://orcid.org/0000-0001-9947-3315
Misawa, Kazuharu https://orcid.org/0000-0002-6277-4330
Miyatake, Satoko https://orcid.org/0000-0001-7587-5168
Mizuguchi, Takeshi https://orcid.org/0000-0003-4998-1244
Matsumoto, Naomichi https://orcid.org/0000-0001-9846-6500
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Text and Data Mining valid from 2025-11-10

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First Online: 10 November 2025

Free to read: This content has been made available to all.