A deletion mutation along with a novel DNA variation in OCRL cause Lowe syndrome in a child with multiple secondary manifestations

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Dades bibliogràfiques
Publicat a:Int J Ophthalmol
Autors principals: Paniri, Alireza, Fattahi, Sadegh, Rasoulinejad, Ahmad, Akhavan-Niaki, Haleh
Format: Artigo
Idioma:Inglês
Publicat: International Journal of Ophthalmology Press 2021
Matèries:
Letter To The Editor
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8025173/
https://ncbi.nlm.nih.gov/pubmed/33875961
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2021.04.25
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