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

Name: Data for: A Familial PLCB4 Mutation Causing Auriculocondylar Syndrome 2 with Variable Severity
Creator: Amira Nabil
Published: 2020-03-27T05:36:36.942Z
Keywords: Sanger Sequencing

Nabil, Amira; El Shakankiri, Nihal; Alkuraya, Fowzan S; Habib, Ahmed; Maddirevula, Sateesh; Morsy, Heba; elshafei, sahar

doi:10.17632/mwszsjbzdf.1

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

Published: 27 March 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

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

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