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Vol. 54. Num. 4.April 2018
Pages 175-240
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Vol. 54. Num. 4.April 2018
Pages 175-240
Letter to the Editor
DOI: 10.1016/j.arbr.2017.10.018
Molecular Detection of the Frequent Allele F52del in Alpha 1 Antitrypsin Deficiency
Detección molecular del alelo F52del frecuente en la deficiencia de alfa-1-antitripsina
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Francisco Martínez Bugalloa,
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fmarbug@gobiernodecanarias.org

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, Juan Marco Figueira Gonçalvesb, María Dolores Martín Martíneza
a Human Genetic Unit, Clinical Analyses Services, University Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain
b Pneumology and Thoracic Surgery Service, University Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain
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Table 1. Genotypes of Subjects with Rare Deficiency Alleles.

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