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Galactosialidosis in a newborn with a novel mutation in the CTSA gene presenting with transient hyperparathyroidism Cover

Galactosialidosis in a newborn with a novel mutation in the CTSA gene presenting with  transient hyperparathyroidism

Balkan Journal of Medical Genetics
Volume 20 (2017): Issue 2 (December 2017)
By: E Okulu,  G Tunc,  T Eminoglu,  O Erdeve,  B Atasay and  S Arsan  
Open Access
|Dec 2017

Authors

E Okulu

emelokulu@gmail.com

Department of Pediatrics, Division of Neonatology, Ankara University School of Medicine, Ankara, Turkey

G Tunc

Department of Pediatrics, Division of Neonatology, Ankara University School of Medicine, Ankara, Turkey

T Eminoglu

Department of Pediatrics, Division of Pediatric Metabolism, Ankara University School of Medicine, Ankara, Turkey

O Erdeve

Department of Pediatrics, Division of Neonatology, Ankara University School of Medicine, Ankara, Turkey

B Atasay

Department of Pediatrics, Division of Neonatology, Ankara University School of Medicine, Ankara, Turkey

S Arsan

Department of Pediatrics, Division of Neonatology, Ankara University School of Medicine, Ankara, Turkey
DOI: https://doi.org/10.1515/bjmg-2017-0031 | Journal eISSN: 2199-5761
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Language: English
Page range: 95 - 97
Published on: Dec 29, 2017
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Galactosialidosis,
Hyperparathyroidism,
Newborn
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2017 E Okulu, G Tunc, T Eminoglu, O Erdeve, B Atasay, S Arsan, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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