reference/28245000

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bibliographicCitation	Aliferis K, Marsal C, Pelletier V, Doray B, Weiss MM, Tops CM, Speeg-Schatz C, Lesnik SA, Dollfus H. A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly. Ophthalmic Genet. 2010 Dec;31(4):205–8. doi: 10.3109/13816810.2010.512355. PMID: 21067481.
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date	2010-11-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/21067481 https://doi.org/10.3109/13816810.2010.512355
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language	English
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title	A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly
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