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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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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2009
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| Assuntos: | |
| Acesso em linha: | 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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