Data for: A Familial PLCB4 Mutation Causing Auriculocondylar Syndrome 2 with Variable Severity

Published: 27-03-2020| Version 1 | DOI: 10.17632/mwszsjbzdf.1
Contributors:
Amira Nabil,
Nihal El Shakankiri,
Fowzan S Alkuraya,
Ahmed Habib,
Sateesh Maddirevula,
Heba Morsy,
sahar elshafei

Description

Sanger sequencing confirmation of the revealed mutation

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