Aspartylglucosaminuria in northern Norway: a molecular and genealogical study.

Aspartylglucosaminuria (AGU, McKusick 208400) is an autosomal recessive lysosomal storage disorder. Ninety percent of all patients are from Finland and only sporadic cases have been reported from elsewhere. In northern Norway, however, nine patients from seven families have been diagnosed with AGU....

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Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Tollersrud, O K, Nilssen, O, Tranebjaerg, L, Borud, O
Materialtyp: Artigo
Språk:Inglês
Publicerad: 1994
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049865/
https://ncbi.nlm.nih.gov/pubmed/8064811
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