Identification of alternatively spliced human biotinidase mRNAs and putative localization of endogenous biotinidase
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference38 articles.
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3. Biotinylation of histones by human serum biotinidase: assessment of biotinyl-transferase activity in sera from normal individuals and children with biotinidase deficiency;Hymes;Biochem. Mol. Med.,1995
4. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency;Wolf;Clin. Chim. Acta,1983
5. Localization of serum biotinidase (BTD) to human chromosome 3 in band p25;Cole;Genomics,1994
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3. Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report;Molecular Case Studies;2018-05-04
4. Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China;American Journal of Medical Genetics Part A;2018-01-23
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