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Test Code 319

Paroxysmal Paralytic Rhabdomyolysis via the LPIN1 Gene, Exons 18-19 Deletion

LPIN1

2 - 3 weeks (8 - 10 days STAT)

Who is this test for?
  • Individuals for whom prior genetic testing was negative or detected a single variant associated with autosomal recessive disease in the relevant gene, and clinical suspicion is high for disease caused by that particular gene 
  • Family members of patients who have tested positive for one of these particular deletions/duplications/inversions
Method
Targeted Deletion
Specimen(s)

Blood, Buccal, Saliva, Tissue

Order Options

OTHER OPTIONS
for pricing.

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