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F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated
F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated
F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated
F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated

F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated

SKU: 42546254203

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F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated

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Description

Mutations in CNNM2 are associated with renal hypomagnesemia

a familial cardiac and skeletal myopathy (CSM)

convenient access to this essential solution for all your experimental needs

Mutations in this gene are associated with HARP syndrome and pantothenate kinase-associated neurodegeneration (PKAN)

Gene Ontology (GO) annotations related to this gene include chromatin binding and RNA polymerase II transcription corepressor activity

F116B Rabbit Polyclonal Antibody, 100ul DNA Fragments Mutations in CNNM2 are associated

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