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KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in
KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in
KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in
KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in

KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in

SKU: 20892874930

4.0
SEK97.20 SEK138.20

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KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in

Store: gaabil.dk · Domain: gaabil.dk

Description

Evidence indicates that mutations in this gene are responsible for the primary defects in patients with progressive myoclonic epilepsy (EPM1)

A pseudogene of this gene is located on the long arm of chromosome 7

subcellular location:In unstimulated cells

This gene is located at the telomeric end of the cystatin locus and encodes a type 2 cystatin-like protein

and a third C-terminal thrombospondin type I repeat (TSP-1)

KLH31 Rabbit Polyclonal Antibody, 20ul Vessels Evidence indicates that mutations in

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