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Test: Glycogen Phosphorylase gene
Alternate names: PYGM
Description:
Clinical: McArdles Disease
Methodology: Common (R49X) caucasian mutation only
Turn around time: 1 month
Transit stability:
Comments:
Sample: Blood EDTA 2 ml, dried blood spots or buccal swabs
Type: Genetics
Method: Point mutation analysis
Consultant/scientist: Ms Surita Meldau
Tel: 021 404 4449
email: surita.meldau@nhls.ac.za
Contact for results: Ms Surita Meldau
Tel: 021 404 4449
email: surita.meldau@uct.ac.za
Delivery address C17 NHLS Labs, NGSH, Observatory, 7925
for samples: Cape Town