Tham khảo STRC

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000242866 - Ensembl, May 2017
  2. ↑ “Human PubMed Reference:”. 
  3. ↑ Verpy E, Masmoudi S, Zwaenepoel I, Leibovici M, Hutchin TP, Del Castillo I, Nouaille S, Blanchard S, Laine S, Popot JL, Moreno F, Mueller RF, Petit C (tháng 11 năm 2001). “Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus”. Nat Genet 29 (3): 345–9. PMID 11687802. doi:10.1038/ng726. 
  4. ↑ Campbell DA, McHale DP, Brown KA, Moynihan LM, Houseman M, Karbani G, Parry G, Janjua AH, Newton V, al-Gazali L, Markham AF, Lench NJ, Mueller RF (tháng 2 năm 1998). “A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22”. J Med Genet 34 (12): 1015–7. PMC 1051155. PMID 9429146. doi:10.1136/jmg.34.12.1015. 
  5. 1 2 “Entrez Gene: STRC stereocilin”. 

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