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J Pediatr Genet 2023; 12(04): e1
DOI: 10.1055/s-0044-1788343
Corrigendum

Corrigendum: A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1

Francisco Cammarata-Scalisi 
1   Departamento of Pediatrics, Regional Hospital of Antofagasta, Antofagasta, Chile
,
Uta Matysiak
2   Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
,
Colin E. Willoughby
3   Genomic Medicine, School of Biomedical Sciences, Ulster University, Northern Ireland, United Kingdom
,
Gunda Ruzaike
2   Department of Pediatrics, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany
,
Antonio Cárdenas Tadich
1   Departamento of Pediatrics, Regional Hospital of Antofagasta, Antofagasta, Chile
,
Maykol Araya Castillo
4   Clinical Laboratory, Regional Hospital of Antofagasta, Chile
,
Carmen Zara-Chirinos
5   Institute of Genetic Research, Faculty of Medicine, University of Zulia, Maracaibo, Venezuela
,
Ana Bracho
5   Institute of Genetic Research, Faculty of Medicine, University of Zulia, Maracaibo, Venezuela
,
Andrea Avendaño
6   Division of Medical Genetics, Department of Pediatrics, Faculty of Medicine, University of Los Andes, Mérida, Venezuela
,
Houweyda Jilani
7   Genetic Department, Mongi Slim Hospital, Marsa, Tunisia
8   Faculty of Medicine of Tunis, University of Tunis El Manar, Tunisia
,
Michele Callea
9   Meyer Children's Hospital, IRCCS, Florence, Italy
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Originalartikel zu diesem Erratum:

A Severe Case of Spondylometaphyseal Dysplasia Algerian Type with Two Mutations in COL2A1J Pediatr Genet 2023; 12(04): 339-341
DOI: 10.1055/s-0041-1732474

It has been brought to the publisher's attention that the affiliation of the last author Michele Callea has been updated. This now correctly reflects in the above article in Journal of Pediatric Genetics, published in Volume 12, Number 04, 339–341 (DOI: 10.1055/s-0041-1732474).



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Artikel online veröffentlicht:
09. Juli 2024

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