Orphanet: Diagnostik der famili�ren hemiplegischen Migr�ne ATP1A2 , CACNA1A und SCN1A Gen
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Diagnosis of familial hemiplegic migraine (ATP1A2, CACNA1A and SCN1A genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 05/12/2012
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Last update: December 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) (3)

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.