Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation

Human gene mutations have revealed that a significant number of ADAMTS (a disintegrin-like and metalloproteinase (reprolysin type) with thrombospondin type 1 motifs) proteins are necessary for normal ocular development and eye function. Mutations in human ADAMTSL4, encoding an ADAMTS-like protein wh...

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Publicat a:Hum Mol Genet
Autors principals: Collin, Gayle B., Hubmacher, Dirk, Charette, Jeremy R., Hicks, Wanda L., Stone, Lisa, Yu, Minzhong, Naggert, Jürgen K., Krebs, Mark P., Peachey, Neal S., Apte, Suneel S., Nishina, Patsy M.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2015
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Articles
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4654052/
https://ncbi.nlm.nih.gov/pubmed/26405179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddv399
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