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:
https://lup.lub.lu.se/record/148118
- author
- Schatz, Patrik
LU
; Ponjavic, Vesna
LU
; Andréasson, Sten
LU
; McGee, Terri L
; Dryja, Thaddeus P
and Abrahamson, Magnus
LU
- organization
- publishing date
- 2005
- 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
- 2016-04-01 15:17:09
- date last changed
- 2022-03-22 03:42:06
@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}},
doi = {{10.1080/13816810500229090}},
volume = {{26}},
year = {{2005}},
}