Clinical DNA Testing

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Laminopathies

Test Descriptions:

Lamin A (LMNA)    Common Mutation for Hutchinson-Gilford Progeria Syndrome

LMNA     Exon Sequencing

Hutchinson-Gilford Progeria Syndrome

Other Tests:  

     Limb-Girdle Muscular Dystrophy

Calpain 3(CAPN3)

Dysferlin Disorder (DYSF)

Fukuyama Congenital Dystrophy, Walker-Warburg Syndrome, Limb Girdle Muscular Dystrophy(FCMD)

Fukutin-Related Protein Disorders (FKRP)

Protein O-Mannosyltransferase 1(POMT1)

Type 2D (SGCA)

Type 2E (SGCB)

Link to Progeria Support Group