Fam83h is Associated with Intracellular Vesicles and ADHCAI

Defects in FAM83H on human chromosome 8q24.3 cause autosomal-dominant hypocalcified amelogenesis imperfecta (ADHCAI). FAM83H does not encode a recognizable signal peptide, so we predicted that the Fam83h protein functions within the cell. We tested this hypothesis by constitutively expressing mouse...

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Bibliografische gegevens
Hoofdauteurs: Ding, Y., Estrella, M.R.P., Hu, Y.Y., Chan, H.L., Zhang, H.D., Kim, J.-W., Simmer, J.P., Hu, J.C.-C.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: SAGE Publications 2009
Onderwerpen:
Research Reports
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2835506/
https://ncbi.nlm.nih.gov/pubmed/19828885
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0022034509349454
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