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Diabetes Metab. 2015 Nov;41(5):433-5. doi: 10.1016/j.diabet.2015.06.003. Epub 2015 Jul 10.

Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome.

Author information

1
Department of Pediatric Endocrinology and Diabetes, Athens Medical Center, 58, av. Kifissias, 15125 Maroussi, Athens, Greece; Pediatric Endocrine Unit, Attikon University Hospital, Athens, Greece. Electronic address: info@pedoendo.gr.
2
Access to Genome, Athens-Thessaloniki, Greece; Department of Medical Genetics, University of Cagliari, Binaghi hospital, Cagliari, Italy.
3
Medical School, Athens University, Athens, Greece.
4
Department of Pediatric Urology, Athens Medical Center, Athens, Greece.
5
Access to Genome, Athens-Thessaloniki, Greece.
6
Department of Medical Genetics, University of Cagliari, Binaghi hospital, Cagliari, Italy.
7
Department of Pediatric Opthalmology, Athens Medical center, Athens, Greece.
8
Department of Pediatric Otorhinolaryngology, Athens Medical center, Athens, Greece.
9
Department of Pediatrics, Athens Medical Center, Athens, Greece.
10
Pediatric Endocrine Unit, Attikon University Hospital, Athens, Greece.
11
Washington University School of Medicine, Saint-Louis, MO, USA.
PMID:
26169481
DOI:
10.1016/j.diabet.2015.06.003
[Indexed for MEDLINE]

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