Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Retinitis Pigmentosa and FSCN2[original query] |
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Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration. Molecular vision 2005 11 (): 922-8. Gamundi María José, Hernan Imma, Maseras Miquel, Baiget Montserrat, Ayuso Carmen, Borrego Salud, Antiñolo Guillermo, Millán José María, Valverde Diana, Carballo Migu |
Allelic copy number variation in FSCN2 detected using allele-specific genotyping and multiplex real-time PCRs. Investigative ophthalmology & visual science 2008 Sep 49 (9): 3799-805. Jin Zi-Bing, Mandai Michiko, Homma Kohei, Ishigami Chie, Hirami Yasuhiko, Nao-I Nobuhisa, Takahashi Masa |
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- Page last updated:Jun 24, 2024
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