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Language : english Subject : anterior eye segment Geographic : united states
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Academic Journal

Localization of SH3PXD2B in human eyes and detection of rare variants in patients with anterior segment diseases and glaucoma.

  • Authors : Mao M; Department of Molecular Physiology and Biophysics, The University of Iowa, Iowa City, IA, USA.; Solivan-Timpe F

Subjects: Polymorphism, Genetic*; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/*genetics ; Anterior Eye Segment/Anterior Eye Segment/Anterior Eye Segment/*pathology Axenfeld-Rieger syndrome

  • Source: Molecular vision [Mol Vis] 2012; Vol. 18, pp. 705-13. Date of Electronic Publication: 2012 Mar 26.Publisher: Molecular Vision Country of Publication: United States NLM ID: 9605351 Publication Model: Print-Electronic Cited

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  • 1-1 of  1 results for ""Eye Diseases, Hereditary""