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Identification of novel mutations in patients with Leber con…
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.
Identification of novel mutations in patients with Leber congenital amaurosis and juvenile RP by genome-wide homozygosity mapping with SNP microarrays.
Article, Chapter
Authors: A.I. den Hollander
Publication: Investigative Ophthalmology and Visual Science, Volume:48, Issue:12, Page(s):5690-5698
Published: Association for Research in Vision and Ophthalmology, 2007
ISSN: 0146-0404
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View Full Text Source:Investigative Ophthalmology and Visual Science,Investigative Ophthalmology and Visual Science,PubMed Central Opens in new Window
Journal:  Investigative Ophthalmology and Visual Science Source:PubMed Central Opens in new Window
Collection:  PubMed Central Opens in new Window
Coverage:
  • 2007~2024-04; volume:48~volume:65;issue:4~2024-04
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