A Novel <i>TBX19</i> Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.

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作者： Nese,Akcan ^[1] ; Nedime,Serakıncı ^[2] ; Burcu,Turkgenc ^[3] ; Ruveyde,Bundak ^[4] ; Nerin,Bahceciler ^[5] ; Sehime G,Temel ^[6]

作者单位： Faculty of Medicine, Department of Pediatric Endocrinology, University of Near East, Nicosia, Cyprus. ^[1] Faculty of Medicine, Department of Medical Genetics, University of Near East, Nicosia, Cyprus. ^[2] Genetic Diagnostic Center, University of Acıbadem, Istanbul, Turkey. ^[3] Faculty of Medicine, Department of Pediatric Endocrinology, University of Kyrenia, Kyrenia, Cyprus. ^[4] Faculty of Medicine, Department of Pediatric Allergy and Immunology, University of Near East, Nicosia, Cyprus. ^[5] Faculty of Medicine, Department of Histology and Embryology, University of Near East, Nicosia, Cyprus. ^[6] Faculty of Medicine, Department of Histology and Embryology, University of Uludag, Bursa, Turkey. ^[7]

关键词 TBX19 gene adrenal insufficiency adrenocorticotropic hormone cortisol respiratory infections

DOI 10.3389/fendo.2017.00064

PMID 28458651

发布时间 2019-11-20

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Frontiers in endocrinology

2017年8卷

64页

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A Novel <i>TBX19</i> Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.

Frontiers in endocrinology

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Frontiers in endocrinology

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A Novel <i>TBX19</i> Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.

Frontiers in endocrinology

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Frontiers in endocrinology

相关期刊

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