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Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.

Schatz, Patrik LU ; Ponjavic, Vesna LU ; Andréasson, Sten LU ; McGee, Terri L; Dryja, Thaddeus P and Abrahamson, Magnus LU (2005) In Ophthalmic Genetics 26(3). p.24-119
Please use this url to cite or link to this publication:
author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Ophthalmic Genetics
volume
26
issue
3
pages
24 - 119
publisher
Taylor & Francis
external identifiers
  • scopus:32044463345
ISSN
1744-5094
DOI
10.1080/13816810500229090
language
English
LU publication?
yes
id
d9992314-89b9-49dd-b547-7091d6852a4c (old id 148118)
alternative location
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16272056&dopt=Abstract
date added to LUP
2007-07-17 09:28:10
date last changed
2017-01-01 06:36:47
@article{d9992314-89b9-49dd-b547-7091d6852a4c,
  author       = {Schatz, Patrik and Ponjavic, Vesna and Andréasson, Sten and McGee, Terri L and Dryja, Thaddeus P and Abrahamson, Magnus},
  issn         = {1744-5094},
  language     = {eng},
  number       = {3},
  pages        = {24--119},
  publisher    = {Taylor & Francis},
  series       = {Ophthalmic Genetics},
  title        = {Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.},
  url          = {http://dx.doi.org/10.1080/13816810500229090},
  volume       = {26},
  year         = {2005},
}