Tissue-specific expression and subcellular localization of ALADIN, the absence of which causes human triple A syndrome

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 disorder (ALADIN). Northern blot analysis sh...

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Bibliografiset tiedot
Päätekijät: Cho, A-Ri, Yang, Keum-Jin, Bae, Yoonsun, Bahk, Young Yil, Kim, Eunmin, Lee, Hyungnam, Kim, Jeong Ki, Park, Wonsang, Rhim, Hyanshuk, Choi, Soo Young, Imanaka, Tsuneo, Moon, Sungdae, Yoon, Jongbok, Yoon, Sungjoo Kim
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Korean Society of Medical Biochemistry and Molecular Biology 2009
Aiheet:
Original Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2705858/
https://ncbi.nlm.nih.gov/pubmed/19322026
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3858/emm.2009.41.6.043
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