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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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| Authors: | Alireza Paniri Sadegh Fattahi Ahmad Rasoulinejad Haleh Akhavan-Niaki |
| Affiliation: | Department of Genetics, Babol University of Medical Sciences, Babol 4717647745, Iran,North Research Center, Pasteur Institute of Iran, Amol 4619332976, Iran,Department of Ophthalmology, Rouhani Hospital, Babol University of Medical Sciences, Babol 4717647745, Iran and Department of Genetics, Babol University of Medical Sciences, Babol 4717647745, Iran; Akhavan-Niaki Genetics Laboratory, Babol 4714957534, Iran |
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