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CG069 Rabbit Polyclonal Antibody, 20ul Centrifuges Mutations in SLC52A2 have been

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CG069 Rabbit Polyclonal Antibody, 20ul Centrifuges Mutations in SLC52A2 have been

Store: avramcheva.com · Domain: avramcheva.com

Description

Mutations in SLC52A2 have been associated with Brown-Vialetto-Van Laere syndrome 2--an autosomal recessive progressive neurologic disorder characterized by deafness

ecently GLUT3 has been identified as a sensitive and specific marker for embyonal carcinomas and yolk tumors

the N-terminal fragment (MST3/N) translocates to the nucleus and promotes programmed cells death

and for interactions with other proteins

Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region

CG069 Rabbit Polyclonal Antibody, 20ul Centrifuges Mutations in SLC52A2 have been

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