Orphanet: Diagnostik der benignen famili�ren infantilen Anf�lle mit Choreoathetosis PRRT2 Gen: Sequenzierung
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Diagnosis of familial infantile convulsions with paroxysmal choreoathetosis (PRRT2 gene: sequencing)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 10/08/2012
  • Phone : 49 (0)89 5160 3683
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Last update: August 2012

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 genes tested (including panels) (1)
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