Affordable Access

Acute intermittent porphyria in Sweden. Molecular, functional and clinical consequences of some new mutations found in the porphobilinogen deaminase gene.

Authors
  • 1
  • 1 Porphyria Centre Sweden, Huddinge University Hospital, Stockholm, Sweden.
Type
Published Article
Journal
Clinical genetics
Publication Date
Volume
62
Issue
4
Pages
288–297
Identifiers
PMID: 12372055
Source
Medline

Abstract

There are no comments yet on this publication. Be the first to share your thoughts.

Statistics

Seen <100 times
0 Comments