Author:
Ohlsson Annika,Guthenberg Claes,Holme Elisabeth,von Döbeln Ulrika
Subject
Genetics (clinical),Genetics
Reference21 articles.
1. Baykal T, Huner G, Sarbat G, Demirkol M (1998) Incidence of biotinidase deficiency in Turkish newborns (letter). Acta Paediatr 87:1102–1103
2. Baykal T, Gokcay G, Gokdemir Y et al (2005) Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of the index case. J Inherit Metab Dis 28:903–912
3. Cole H, Reynolds TR, Lockyer JM et al (1994a) Human serum biotinidase: cDNA cloning, sequence, and characterization. J Biol Chem 269:6566–6570
4. Cole H, Weremowicz S, Morton CC, Wolf B (1994b) Localization of serum biotinidase (BTD) to human chromosome 3 in band p25. Genomics 22:662–663
5. Elsas LJ, Dembure PP, Langley S et al (1994) A common mutation associated with the Duarte galactosemia allele. Am J Hum Genet 54:1030–1036
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