Publishing research using ab74415? Please let us know so that we can cite the reference in this datasheet.

ab74415 has been referenced in 1 publication.

  • Girotto G  et al. Linkage study and exome sequencing identify a BDP1 mutation associated with hereditary hearing loss. PLoS One 8:e80323 (2013). IHC-P ; Mouse . PubMed: 24312468

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