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Deletion/insertion mutation that causes biotinidase deficiency may result from the formation of a quasipalindromic structure.
Pomponio, R J; Narasimhan, V; Reynolds, T R; Buck, G A; Povirk, L F; Wolf, B.
Affiliation
  • Pomponio RJ; Human Genetics, Medical College of Virginia, Virginia Commonwealth University, Richmond, USA.
Hum Mol Genet ; 5(10): 1657-61, 1996 Oct.
Article in En | MEDLINE | ID: mdl-8894703
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Database: MEDLINE Main subject: Chromosomes, Human, Pair 3 / Chromosomes, Human, Pair 7 / Amidohydrolases Type of study: Etiology_studies / Prognostic_studies Limits: Humans / Infant / Male Language: En Year: 1996 Type: Article
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Database: MEDLINE Main subject: Chromosomes, Human, Pair 3 / Chromosomes, Human, Pair 7 / Amidohydrolases Type of study: Etiology_studies / Prognostic_studies Limits: Humans / Infant / Male Language: En Year: 1996 Type: Article