Hurler’s syndrome: dental findings in a case treated with bone marrow transplantation in infancy
Author
: E. J. HINGSTON, M. L. HUNTER, B. HUNTER, & N. DRAGE
Publisher
: Paediatric Dentistry
Summary :Hurler’s syndrome, also known as mucopolysaccharidosis I (MPS I-H), is a rare condition inherited as an autosomal recessive trait.
Copies :
No. |
Barcode |
Location |
No. Shelf |
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1 |
08195099 |
Ruang Referensi - Perpustakaan FKIK |
01 |
TIDAK DIPINJAMKAN |