TWO OPPOSITE PHENOTYPES OF GLUCOSE DISORDERS IN A FAMILY WITH HETEROZYGOUS P.SER453LEU (C.1358C> T) MUTATION IN THE GLUCOKINASE (GCK) GENE: MATURITY ONSET DIABETES IN YOUNG AND INSULINOMA.

Demiral, M; Çelebi, H B G; Cander, S; Yerci, O; Eren, E; Demirbilek, H

Demiral, M; Çelebi, H B G; Cander, S; Yerci, O; Eren, E; Demirbilek, H.

Afiliação

Demiral M; Balikesir Atatürk City Hospital, Department of Paediatric Endocrinology, Balikesir.
Çelebi HBG; Balikesir Atatürk City Hospital, Department of Medical Genetic, Balikesir.
Cander S; Uludag University, Department of Endocrinology, Bursa.
Yerci O; Uludag University, Department of Pathology, Bursa.
Eren E; Uludag University, Department of Paediatric Endocrinology, Bursa.
Demirbilek H; Hacettepe University, Faculty of Medicine, Department of Paediatric Endocrinology, Ankara, Turkey.

Acta Endocrinol (Buchar) ; 18(4): 458-465, 2022.

Article em En | MEDLINE | ID: mdl-37152879

Palavras-chave

GCK gene; MODY; hyperinsulinaemic hypoglycaemia; insulinoma

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Acta Endocrinol (Buchar) Ano de publicação: 2022 Tipo de documento: Article

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