Orphanet: Molekulare Diagnostik der benignen famili�ren infantilen Epilepsie KCNQ2, KCNQ3, PRRT2 und SCN2A Gen
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Molecular diagnosis of benign familial infantile epilepsy (KCNQ2, KCNQ3, PRRT2, and SCN2A genes)

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Last update: December 2017

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (4)
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