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United States Targeted Detection Program for Alpha-1 Antitrypsin Deficiency

  • Tonelli A
  • Rouhani F
  • Brantly M
DOI: 10.1007/978-3-319-23449-6_5
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Abstract

Alpha-1 antitrypsin deficiency (AATD) is a hereditary condition in which less than 10 % of the individuals are identified. This under-recognition is a barrier to lifestyle modifications, genetic...

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Tonelli, A. R., Rouhani, F., & Brantly, M. L. (2016). United States Targeted Detection Program for Alpha-1 Antitrypsin Deficiency (pp. 85–98). https://doi.org/10.1007/978-3-319-23449-6_5

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