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Article Abstract
Not much is known about FAM136A, a human gene that may be involved in Meniere's disease and is conserved throughout animals. To understand the function of , the ortholog of FAM136A, loss of function alleles of the gene were generated. We find that loss of function results in minor but significant changes to the locomotion and behavior.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9163966 | PMC |
| http://dx.doi.org/10.17912/micropub.biology.000553 | DOI Listing |
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