Identification of a novel mutation of the SHOX gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency.

Kang, Jaebeen; Kim, Min-Ji; Yoo, Sukdong; Cheon, Chong Kun

Kang, Jaebeen; Kim, Min-Ji; Yoo, Sukdong; Cheon, Chong Kun.

Affiliation

Kang J; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea.
Kim MJ; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea.
Yoo S; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea.
Cheon CK; Department of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, Korea.

Ann Pediatr Endocrinol Metab ; 29(3): 201-203, 2024 Jun.

Article de En | MEDLINE | ID: mdl-38956755

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Ann Pediatr Endocrinol Metab Année: 2024 Type de document: Article Pays de publication: Corée du Sud

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