Meeting abstract

https://doi.org/10.26800/LV-144-supl7-10

Case report: Pitt-Hopkins like syndrome with CNTNAP2 mutation in three siblings

Marta Grgat
Barbara Goršeta
Viktorija Antolović

Abstract

Keywords

CNTNAP2, developmental delay, epilepsy, paediatrics, Pitt Hopkins-like syndrome 1

Hrčak ID:

291757

URI

https://hrcak.srce.hr/291757

Publication date:

28.12.2022.

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