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Connexin 26 R143W Mutation Associated with Recessive Nonsyndromic Sensorineural Deafness in Africa

  • Brobby G
  • Müller-Myhsok B
  • Horstmann R
New England Journal of Medicine (1998) 338(8) 548-550
DOI: 10.1056/nejm199802193380813
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Abstract

A letter to the editor is presented discussing mutation of connexin 26 R143W associated with recessive nonsyndromic sensorineural deafness in Africa.

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APA

Brobby, G. W., Müller-Myhsok, B., & Horstmann, R. D. (1998). Connexin 26 R143W Mutation Associated with Recessive Nonsyndromic Sensorineural Deafness in Africa. New England Journal of Medicine, 338(8), 548–550. https://doi.org/10.1056/nejm199802193380813

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