Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: 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 |
Population-scale analysis of common and rare genetic variation associated with hearing loss in adults.
Communications biology 2022 06 5 (1): 540. Praveen Kavita, Dobbyn Lee, Gurski Lauren, Ayer Ariane H, Staples Jeffrey, Mishra Shawn, Bai Yu, Kaufman Alexandra, Moscati Arden, Benner Christian, Chen Esteban, Chen Siying, Popov Alexander, Smith Janell, , , , Melander Olle, Jones Marcus B, Marchini Jonathan, Balasubramanian Suganthi, Zambrowicz Brian, Drummond Meghan C, Baras Aris, Abecasis Goncalo R, Ferreira Manuel A, Stahl Eli A, Coppola Giovan |
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