Orphanet: Diagnostik des Dravet Syndroms und anderer SCN1A assoziierter Erkrankungen SCNA1 Gen: Sequenzierung, MLPA
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Diagnosis of Dravet syndrome and other SCN1A-associated diseases (SCNA1 gene: : sequencing, MLPA)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 16/04/2015
  • Phone : 49 (0)40 53805 853
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  • Fax : 49 (0)40 53805 821
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Last update: April 2015

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Deletion / Duplication analysis
MLPA based techniques

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.