TNFSF14 Polyclonal Antibody-BS61000 Affinity IHH gene mutations cause the

IHH gene mutations cause the brachydactyly type A1 which is characterized by shortening or malformation of the phalanges and also the acrocapitofemoral dysplasia

The gene encoding RTDR1 maps to human chromosome 22

Gene Name: TCEA3

Gene Name: EXOSC9

Background: This gene encodes a member of a small family of guanosine triphosphate (GTP) metabolizing proteins that contain a CRIB (Cdc42

TNFSF14 Polyclonal Antibody-BS61000 Affinity IHH gene mutations cause theTNFSF14 Polyclonal Antibody Catalogue Numbers: BS61000 50, BS61000 100 Sizes: 50l, 100l Alternative Name: Tumor necrosis factor ligand superfamily member 14; Herpes virus entry mediator ligand; HVEM L; Herpesvirus entry mediator ligand; CD258; Cleaved into the following 2 chains; Tumor necrosis factor ligand superfamily member 14, membrane form; Tumor necrosis factor ligand superfamily member 14, soluble form; TNFSF14; HVEML; LIGHT; UNQ391; PRO726