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A novel mutation in a newborn baby leading to glycogen storage disease type Ia

S Dorum

S Dorum

Department of Pediatrics, Division of Metabolism, Bursa Yuksek Ihtisas Training and Research HospitalBursa, Turkey
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Dorum, S
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O Gorukmez

O Gorukmez

Department of Genetics, Bursa Yuksek Ihtisas Training and Research HospitalBursa, Turkey
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Gorukmez, O
  
31 déc. 2018
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Catégorie d'article: Case Report
Publié en ligne: 31 déc. 2018
Pages: 55 - 57
DOI: https://doi.org/10.2478/bjmg-2018-0018
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© 2018 Dorum S, Gorukmez O, published by Sciendo
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

Figure 1

Sequencing analysis of the G6PC gene c.137T>G mutation. (a) The arrow shows the site of the homozygous c.137T>G mutation in the G6PC gene of the patient. (b) Heterozygous mutation carrier (mother). (c) Heterozygous mutation carrier (father).
Sequencing analysis of the G6PC gene c.137T>G mutation. (a) The arrow shows the site of the homozygous c.137T>G mutation in the G6PC gene of the patient. (b) Heterozygous mutation carrier (mother). (c) Heterozygous mutation carrier (father).
Langue:
Anglais
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2 fois par an
Sujets de la revue:
Médecine, Sciences médicales de base, Sciences médicales de base, autres
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