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. 2025 Sep 12;112(10):2562. doi: 10.1016/j.ajhg.2025.09.005

Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes

David Heimdörfer ∗, Alexander Vorleuter, Alexander Eschlböck, Angeliki Spathopoulou, Marta Suarez-Cubero, Hesso Farhan, Veronika Reiterer, Melanie Spanjaard, Christian P Schaaf, Lukas A Huber, Leopold Kremser, Bettina Sarg, Frank Edenhofer, Stephan Geley, Mariana EG de Araujo, Alexander Huettenhofer ∗∗
PMCID: PMC12808939  PMID: 40945516

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(The American Journal of Human Genetics 111, 1383–1404; July 11, 2024)

In the originally published Figure 5D, we reported "RPL15" in the list of proteins. This is a typo and has been corrected to be "MRPL15." Additionally, the original legend for Figure 5C read "...and those identified in 2 of 3 replicates of the BioID or GFP-CoIP ..." This has been corrected to be "...and those identified in at least 2 of 3 replicates of the BioID or GFP-CoIP ..."

Figure 5.

Figure 5

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SNORD116 does not directly interact with WT MAGEL2 or p.Gln666Profs∗47, corrected

Contributor Information

David Heimdörfer, Email: david.heimdoerfer@i-med.ac.at.

Alexander Huettenhofer, Email: alexander.huettenhofer@i-med.ac.at.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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