Orphanet: Molecular diagnosis of Progressive Myoclonic Epilepsy type 3, 4, 5 and 6 KCTD7, SCARB2, PRICKLE2 and GOSR2 gene
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Molecular diagnosis of Progressive Myoclonic Epilepsy type 3, 4, 5 and 6 (KCTD7, SCARB2, PRICKLE2 and GOSR2 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 05/03/2014
  • Phone : +31 (0)88 755 4090
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Last update: March 2014

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
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