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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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| Autori principali: | , , , , , , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Korean Society of Medical Biochemistry and Molecular Biology
2009
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| Soggetti: | |
| Accesso online: | 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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