(Q45105843)
Statements
1 reference
Mutation (Q456H) is the most common cause of profound biotinidase deficiency in children ascertained by newborn screening in the United States (English)
1 reference
Norrgard KJ
1 reference
Pomponio RJ
1 reference
Swango KL
1 reference
Hymes J
1 reference
Reynolds TR
1 reference
Buck GA
1 reference
Wolf B
1 reference
1 June 1997
1 reference
1 reference
61
1 reference
1
1 reference
22-27
1 reference
Identifiers
1 reference
1 reference