Expanding the Phenotype of <i>TRMT10A</i> Mutations: Case Report and a Review of the Existing Cases

Siklar, Zeynep; Kontbay, Tugba; Colclough, Kevin; Patel, Kashyap A.; Berberoglu, Merih

Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases

Siklar, Zeynep; Kontbay, Tugba; Colclough, Kevin; Patel, Kashyap A.; Berberoglu, Merih.

Affiliation

Siklar Z; Ankara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey
Kontbay T; Ankara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey
Colclough K; Exeter Genomics Laboratory, Royal Devon and Exeter Hospital, Exeter, UK
Patel KA; University of Exeter, College of Medicine and Health, Exeter, UK
Berberoglu M; Ankara University Faculty of Medicine, Department of Pediatric Endocrinology, Ankara, Turkey

J Clin Res Pediatr Endocrinol ; 15(1): 90-96, 2023 02 27.

Article de En | MEDLINE | ID: mdl-34541035

Mots clés

TRMT10A; monogenic diabetes; ovarian failure

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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: J Clin Res Pediatr Endocrinol Année: 2023 Type de document: Article Pays d'affiliation: Turquie

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