LPPRC Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Mutations in this gene are

Mutations in this gene are a cause of Cushing disease and adrenocortical hyperplasia

GDF7 encodes a member of the bone morphogenetic protein (BMP) family

interacting with gamma-tubulin to help regulate proper centrosome function

G34 and G17

inhibition of neuroblastoma cell differentiation

LPPRC Rabbit Polyclonal Antibody, 50ul Nucleic Acid Isolation & Purification Mutations in this gene areThis gene encodes a leucine rich protein that has multiple pentatricopeptide repeats (PPR). The precise role of this protein is unknown but studies suggest it may play a role in cytoskeletal organization vesicular transport or in transcriptional regulation of both nuclear and mitochondrial genes. The protein localizes primarily to mitochondria and is predicted to have an N terminal mitochondrial targeting sequence. Mutations in this gene are