Genetic Association Analysis in a Clinically and Histologically Confirmed Otosclerosis Population Confirms Association With the TGFB1 Gene but Suggests an Association of the RELN Gene With a Clinically Indistinguishable Otosclerosis-Like Phenotype
Manou Sommen; Guy Van Camp; Balázs Liktor; Péter Csomor; Erik Fransén; István Sziklai; Isabelle Schrauwen; Tamás Karosi · 2014 · Otology & Neurotology
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
BACKGROUND/HYPOTHESIS: Otosclerosis is a frequent cause of hearing impairment characterized by abnormal resorption and deposition of bone in the human otic capsule. It is a disease of complex etiopathogenesis that is caused by both…
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Metadata source: OpenAlex · DOI 10.1097/mao.0000000000000334