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Test Code 15227

Spastic Paraplegia 3A via the ATL1 Gene

ATL1

N/A

Who is this test for?

Individuals with symptoms consistent with autosomal dominant HSP (particularly the ones with early-onset), and family members of patients who have known ATL1-HSP mutations are ideal candidates for this test.

Method
Sequencing with CNV PG-Select
Specimen(s)

Blood, Saliva, or Buccal Swab

Order Options

Test type
OTHER OPTIONS
for standard institutional pricing.

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