FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos also known as X-linked recessive

also known as X-linked recessive Charcot-Marie-Tooth disease-4 (CMTX-4)

insulin resistance

Component of the probable ECS(SPSB4) complex with the substrate recognition component SPSB4

CDH7 is present in a gene cluster on chromosome 18

GRIN2A encodes a member of the glutamate-gated ion channel protein family

FANCL Polyclonal Antibody, 100ul Diagnostic Probes & Oligos also known as X-linked recessiveThe 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