- Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome
-
Cho AR, Yang KJ, Bae Y, Bahk YY, Kim E, Lee H, Kim JK, Park W, Rhim H, Choi SY, Imanaka T, Moon S, Yoon J, Yoon SK
- KMID: 756230
- Exp Mol Med.
- 2009 Jun;41(6):381-386.
- doi: 10.3858/emm.2009.41.6.043
Triple A syndrome is a rare genetic disorder caused by mutations in the achalasia-addisonianism-alacrima syndrome (AAAS) gene which encodes a tryptophan aspartic acid (WD) repeat-containing protein named alacrima-achalasia-adrenal insufficiency neurologic... -
- CITED
-
- Close
- SHARE
-
- Close
