Orphanet: Molekulare Diagnostik der fr�hinfantilen epileptischen Enzephalopathie ARX, CDKL5, HCN1, SCN2A und STXBP1 Gen

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Molecular diagnosis of early infantile epileptic encephalopathy (ARX, CDKL5, HCN1, SCN2A, and STXBP1 genes)

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Last update: November 2017

Responsible of diagnostic test


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) (5)
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