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Pejvakin 产品

(Deafness, Autosomal Recessive 59 (DFNB59))

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The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). [provided by RefSeq, Dec 2008].

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Featured Pejvakin Categories

Pejvakin 抗体

High quality antibodies with extensive validation data.

Pejvakin 蛋白

Proteins for various applications incl. WB, ELISA, IF etc.

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Synonyms and alternative names related to Pejvakin

deafness, autosomal recessive 59 (DFNB59), pejvakin (PJVK), pejvakin (Pjvk), Gm1001, PJVK, Pjvk

Protein level used designations for Pejvakin

  • deafness, autosomal recessive 59
  • pejvakin
  • pejvakin-like
  • autosomal recessive deafness type 59 protein
  • autosomal recessive deafness type 59 protein homolog
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