Impaired oral health in patients with aspartylglucosaminuria

Author:

Arvio Pekka,Arvio Maria,Wolf Juhani,Lukinmaa Pirjo-Liisa,Saxen Leena,Pirinen Sinikka

Publisher

Elsevier BV

Subject

General Dentistry,Otorhinolaryngology,Oral Surgery,Surgery

Reference28 articles.

1. Aspartylglycosaminuria in the Finnish population: identification of two point mutations in the heavy chain of glycoasparaginase;Mononen,1991

2. Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease;Ikonen;EMBO J,1991

3. Functional analyses of active site residues of human lysosomal aspartylglucosaminidase: implications for catalytic mechanism and autocatalytic activation;Tikkanen;EMBO J,1996

4. Gene defects causing aspartylglycosaminuria;Park,1997

5. Early clinical symptoms and incidence of aspartylglucosaminuria in Finland;Arvio;Acta Paediatr,1993

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