Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes

Solve-RD consortium

doi:10.1038/s41431-025-01841-w

Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes

Solve-RD consortium

Division of Evolution, Infection and Genomics

Research output: Contribution to journal › Article

Original language	English
Number of pages	3
Journal	European journal of human genetics : EJHG
DOIs	https://doi.org/10.1038/s41431-025-01841-w
Publication status	Published - 7 Apr 2025

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10.1038/s41431-025-01841-wLicence: CC BY

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title = "Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes",

author = "\{Solve-RD consortium\} and German Demidov and Steven Laurie and Annalaura Torella and Giulio Piluso and Marcello Scala and Manuela Morleo and Vincenzo Nigro and Holm Graessner and Siddharth Banka and Katja Lohmann and Stephan Ossowski",

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AU - Solve-RD consortium

AU - Demidov, German

AU - Laurie, Steven

AU - Torella, Annalaura

AU - Piluso, Giulio

AU - Scala, Marcello

AU - Morleo, Manuela

AU - Nigro, Vincenzo

AU - Graessner, Holm

AU - Banka, Siddharth

AU - Lohmann, Katja

AU - Ossowski, Stephan

PY - 2025/4/7

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JO - European journal of human genetics : EJHG

JF - European journal of human genetics : EJHG

ER -

Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes

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