FANCD2 Polyclonal Antibody, 20ul Micro Centrifuge Tubes Mutations in SPTAN1 are the

Mutations in SPTAN1 are the cause of early infantile epileptic encephalopathy-5

One mechanism of foreign DNA restriction is deamination of foreign double-stranded DNA cytidines to uridines

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This apolipoprotein L family member may play a role in lipid exchange and transport throughout the body

Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene

FANCD2 Polyclonal Antibody, 20ul Micro Centrifuge Tubes Mutations in SPTAN1 are theThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal