Prevalence of STRC variants among mild-moderate hearing loss or presumptive autosomal recessive inheritance in the Brazilian population

Author(s)

Diogo-Cavassana, Stella ; Alencar-Coutinho, Danillo ; Anjos-Monteiro, Allan ; Pailo-Carvalho, Thais ; Murano, Emi Z. ; Oiticica, Jeanne ; Bento, Ricardo F. ; Mingroni-Netto, Regina ; Batissoco, Ana Carla ; Lezirovitz, Karina

• Document type: Journal article
• Source: European Journal of Human Genetics; v. 32, p. 1-pg., 2024-12-01.
• FAPESP's process: 23/07188-7 - Investigation of new hereditary forms of hearing loss and its pathophysiological mechanism
• Grantee: Karina Lezirovitz Mandelbaum
• Support Opportunities: Regular Research Grants
• FAPESP's process: 13/08028-1 - CEGH-CEL - Human Genome and Stem Cell Research Center
• Grantee: Mayana Zatz
• Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC