✦ LIBER ✦

Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria

✍ Scribed by Klemens Frei; Reinhard Ramsebner; Gertrude Hamader; Trevor Lucas; Christian Schoefer; Wolf-Dieter Baumgartner; Franz J Wachtler; Karin Kirschhofer

Book ID: 116524579
Publisher: Elsevier Science
Year: 2004
Tongue: English
Weight: 204 KB
Volume: 194
Category: Article
ISSN: 0378-5955
DOI: 10.1016/j.heares.2004.03.007

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A mutation in GJB3 is associated with re

A mutation in GJB3 is associated with recessive erythrokeratodermia variabilis (EKV) and leads to defective trafficking of the connexin 31 protein

✍ Gottfried, I. 📂 Article 📅 2002 🏛 Oxford University Press 🌐 English ⚖ 1004 KB

Lack of association between a functional

Lack of association between a functional genetic variant of connexin 37 and ischemic stroke in a Taiwanese population

✍ Suh-Hang Hank Juo; Yi-Chu Liao; Hsiu-Fen Lin; Po-Lin Chen; Wen-Yi Lin; Ruey-Tay 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 158 KB

Lack of association between pro-inflamma

Lack of association between pro-inflammatory genotypes of the interleukin-1 (IL-1B -31 C/+ and IL-1RN *2/*2) and gastric cancer/duodenal ulcer in Korean population

✍ Seong-Gene Lee; Byungsik Kim; Wonyong Choi; Inchul Lee; Jaewon Choi; Kyuyoung So 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 90 KB