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Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion


Morscher, Raphael Johannes; Rauscher, Christian; Sperl, Wolfgang; Rittinger, Olaf (2017). Seizures, enamel defects and psychomotor developmental delay: The first patient with Kohlschütter-Tönz syndrome caused by a ROGDI-gene deletion. Seizure, 50:118-120.

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Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Children's Hospital Zurich > Medical Clinic
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Life Sciences > Neurology
Health Sciences > Neurology (clinical)
Language:English
Date:August 2017
Deposited On:12 Mar 2019 16:13
Last Modified:28 Jul 2020 14:07
Publisher:Elsevier
ISSN:1059-1311
OA Status:Hybrid
Free access at:Publisher DOI. An embargo period may apply.
Publisher DOI:https://doi.org/10.1016/j.seizure.2017.06.017
PubMed ID:28651123

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