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Brain. 2017 Aug 1;140(8):e49. doi: 10.1093/brain/awx155.

The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders.

Author information

1
Department of Molecular Neuroscience, Institute of Neurology, UCL Institute of Neurology, London WC1N 3BG, UK.
2
Department of Molecular Medicine and Medical Biotechnologies "DMMBM", University of Naples "Federico II", Naples 80131, Italy.
3
CEINGE Biotecnologie Avanzate, Naples 80131, Italy.
4
European School of Molecular Medicine, SEMM, University of Milan, Italy.
5
King Saud bin Abdulaziz University for Health Sciences, Department of Pediatrics, Division of Genetics, Riyadh 14611, Saudi Arabia.
6
Genetics and Rare Diseases Research Division, Ospedale Pediatrico "Bambino Gesù", Rome 00146, Italy.
PMID:
28899015
PMCID:
PMC5806505
DOI:
10.1093/brain/awx155
[Indexed for MEDLINE]
Free PMC Article

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