Sanger Sequencing of the TRPV4 gene

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Documentation:
Ref: LV2072 Categories: , , , , , , , , , , , Diseases: Brachyolmia type 3,Digital arthropathy-brachydactyly, familial,Hereditary motor and sensory neuropathy, type IIc,Metatropic dysplasia,Parastremmatic dwarfism,Scapuloperoneal spinal muscular atrophy,Spinal muscular atrophy, distal, congenital nonprogressive,SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE,Spondylometaphyseal dysplasia, Kozlowski type,TRPV4 group: Metatropic dysplasia, Spondyloepimetaphyseal dysplasia, Maroteaux type, Spondylometaphyseal dysplasia, Kozlowski type, Brachyolmia, Familial digital arthropathy with brachydactylyGenes: TRPV4Delivery term: 35 days
sistemas genómicos
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