Double homozygous Cystic Fibrosis Transmembrane Regulator gene (CFTR) mutation: A case series and review of the literature
<p>Introduction: Double homozygous mutation with the presence of double mutations in each allele is a very rare phenomenon with only 2 reports that have described this phenomenon in the medical literature.</p><p>Objective: To find the prevalence of double homozygous in our Cf popul...
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| Formaat: | Boek |
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Global Journal of Rare Diseases - Peertechz Publications,
2020-08-18.
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A1234.567 |
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| Kopie 1 | Beschikbaar |