K. Jensen

Three dimensional structure of human biotinidase: computer modeling and functional correlations.

K. Pindolia, B. Wolf, K. Jensen, 2007, Molecular Genetics and Metabolism.

Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases

B. Wolf, Y. Gokdemir, G. Gokçay, 2005, Journal of Inherited Metabolic Disease.

Evolutionary conservation of biotinidase: implications for the enzyme's structure and subcellular localization.

B. Wolf, K. Jensen, 2005, Molecular genetics and metabolism.

Biotinidase deficiency: Novel mutations and their biochemical and clinical correlates

D. Goudie, M. Blitzer, Helio F. Pedro, 2005, Human mutation.

Newborn screening for biotinidase deficiency in Brazil: biochemical and molecular characterizations.

E. C. Neto, R. Giugliani, B. Wolf, 2004, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Seventeen novel mutations that cause profound biotinidase deficiency.

T. Suormala, E. R. Baumgartner, C. Pérez-Cerdá, 2002, Molecular genetics and metabolism.

Hearing loss in biotinidase deficiency: genotype-phenotype correlation.

T. Coşkun, B. Wolf, A. Dursun, 2007, The Journal of pediatrics.

MUTATION IN BRIEF

Sharon Quary, A. Slonim, T. Baykal, 2022 .