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Mutations in VMD2 cause autosomal dominant vitreoretinochoroidopathy (ADVIRC)

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Chicago
Leroy, Bart, J YARDLEY, N HART-HOLDEN, Bart Lafaut, B PUECH, MA REDDY, Jean Delaey, Philippe Kestelyn, AT MOORE, and GCM BLACK. 2005. “Mutations in VMD2 Cause Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC).” In Investigative Ophthalmology & Visual Science. Vol. 46. ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
APA
Leroy, Bart, YARDLEY, J., HART-HOLDEN, N., Lafaut, B., PUECH, B., REDDY, M., Delaey, J., et al. (2005). Mutations in VMD2 cause autosomal dominant vitreoretinochoroidopathy (ADVIRC). INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (Vol. 46). ASSOC RESEARCH VISION OPHTHALMOLOGY INC.
Vancouver
1.
Leroy B, YARDLEY J, HART-HOLDEN N, Lafaut B, PUECH B, REDDY M, et al. Mutations in VMD2 cause autosomal dominant vitreoretinochoroidopathy (ADVIRC). INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. ASSOC RESEARCH VISION OPHTHALMOLOGY INC; 2005.
MLA
Leroy, Bart, J YARDLEY, N HART-HOLDEN, et al. “Mutations in VMD2 Cause Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC).” Investigative Ophthalmology & Visual Science. Vol. 46. ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2005. Print.
@inproceedings{327502,
  author       = {Leroy, Bart and YARDLEY, J and HART-HOLDEN, N and Lafaut, Bart and PUECH, B and REDDY, MA and Delaey, Jean and Kestelyn, Philippe and MOORE, AT and BLACK, GCM},
  booktitle    = {INVESTIGATIVE OPHTHALMOLOGY \& VISUAL SCIENCE},
  issn         = {0146-0404},
  language     = {eng},
  publisher    = {ASSOC RESEARCH VISION OPHTHALMOLOGY INC},
  title        = {Mutations in VMD2 cause autosomal dominant vitreoretinochoroidopathy (ADVIRC)},
  volume       = {46},
  year         = {2005},
}

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