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Acta Neurol Belg. 2018 Oct 8. doi: 10.1007/s13760-018-1026-5. [Epub ahead of print]

A new NBIA patient from Turkey with homozygous C19ORF12 mutation.

Author information

1
Department of Pediatric Metabolism and Nutrition, Dr. Sami Ulus Maternity and Children's Research and Education Hospital, Ankara, Turkey. cskasapkara@gmail.com.
2
Department of Pediatric Metabolism and Nutrition, Gazi University Hospital, Ankara, Turkey.
3
Molecular and Medical Genetics, Pediatrics and Neurology, Oregon Health and Science University, Portland, Oregon, 97239, USA.
4
Department of Pediatric Radiology, Dr. Sami Ulus Maternity and Children's Research and Education Hospital, Ankara, Turkey.
PMID:
30298423
DOI:
10.1007/s13760-018-1026-5

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