In silico prediction of functional loss of cst3 gene in hereditary cerebral amyloid angiopathy

The computational identification of missense mutation in CST3 (CYSTATIN 3 or CYSTATIN C) gene has been done in the present study. The missense mutations in the CST3 gene will leads to hereditary cerebral amyloid angiopathy  The initiation of the analysis was done with SIFT followed by POLYPHEN-2 and...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Piyush Choudhary (Egilea), Juhee Singh (Egilea), V. Karthick (Egilea), V. Shanthi (Egilea), R. Rajasekaran (Egilea), Karuppasamy Ramanathan (Egilea)
Formatua: Liburua
Argitaratua: Bangladesh Pharmacological Society, 2013-11-01T00:00:00Z.
Gaiak:
Sarrera elektronikoa:Connect to this object online.
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Internet

Connect to this object online.

3rd Floor Main Library

Aleari buruzko argibideak 3rd Floor Main Library
Sailkapena: A1234.567
Alea 1 Eskuragarri