Haemophilia A and mucopolysaccharidosis I-H (Hurler Syndrome): a case report.

Benedik-Dolnicar M., Strmecki L., Paschke E., Steglich C., Kranjc O., Komel R.

Type

Journal article

Publication Date

2002-08-01T00:00:00+00:00

Volume

87

Keywords

Child, Preschool, Chromosome Inversion, Codon, Nonsense, DNA Mutational Analysis, Europe, Factor VIII, Female, Gene Frequency, Genetic Carrier Screening, Hemophilia A, Humans, Iduronidase, Incidence, Male, Mucopolysaccharidosis I, Point Mutation, Pregnancy, Pregnancy Complications, Slovenia

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