作者：
Gerarda,Cappuccio [1]
;
Margherita Lucia,De Bernardi [2]
;
Alessia,Morlando [1]
;
Cristina,Peduto [1]
;
Iris,Scala [3]
;
Michele,Pinelli [1]
;
Emanuele,Bellacchio [1]
;
Flavio Gioele,Gallo [4]
;
Adriano,Magli [5]
;
Carmen,Plaitano [6]
;
Mercedes,Serrano [6]
;
Leticia,Pías [7]
;
Jaume,Català [8]
;
Mercè,Bolasell [9]
;
Annalaura,Torella [8]
;
Vincenzo,Nigro [8]
;
Ginevra,Zanni [9]
;
Nicola,Brunetti-Pierri [2]
作者单位：
Department of Translational Medicine, Section of Pediatrics, Federico II University, Naples, Italy.
[1]
Telethon Institute of Genetics and Medicine, Naples, Italy.
[2]
Department of Precision Health, University of Campania 'Luigi Vanvitelli', Naples, Italy.
[3]
Department of Molecular Medicine and Medical Biotechnology (DMMBM), Federico II University, Naples, Italy.
[4]
Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, Rome, Italy.
[5]
Department of Pediatric Ophthalmology, University of Salerno, Fisciano, Italy.
[6]
Department of Ophthalmology, A.O.U. San Giovanni Di Dio e Ruggi d'Aragona-Scuola Medica Salernitana, Salerno, Italy.
[7]
Department of Ophthalmology and Department of Genetic and Molecular Medicine, Hospital Sant Joan de Déu, Barcelona, Spain.
[8]
U-703 Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, Madrid, Spain.
[9]
Unit of Muscular and Neurodegenerative Diseases, Department of Neurosciences, Bambino Gesù Children's Hospital, Rome, Italy.
[10]
DOI
10.1002/ajmg.a.62911
PMID
35876338
发布时间
2023-01-30
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