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RESEARCH ARTICLE
A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
Ashlee J. Conway, Fiona C. Brown, Robert O. Fullinfaw, Benjamin T. Kile, Stephen M. Jane, David J. Curtis
Disease Models & Mechanisms 2017 10: 1005-1013; doi: 10.1242/dmm.029116
Ashlee J. Conway
1Australian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia
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Fiona C. Brown
1Australian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia
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Robert O. Fullinfaw
2Porphyria Reference Laboratory, Biochemistry Department, Royal Melbourne Hospital, Parkville 3050, Australia
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Benjamin T. Kile
3ACRF Chemical Biology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville 3052, Australia
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  • ORCID record for Benjamin T. Kile
Stephen M. Jane
1Australian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia
4Central Clinical School, Monash University, Melbourne 3004, Australia
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David J. Curtis
1Australian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia
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  • For correspondence: david.curtis@monash.edu
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Article Information

vol. 10 no. 8, 1005-1013

DOI 
https://doi.org/10.1242/dmm.029116
PubMed 
28600349

Published By 
The Company of Biologists Ltd
Print ISSN 
1754-8403
Online ISSN 
1754-8411
History 
  • Received December 25, 2016
  • Accepted June 2, 2017
  • Published online August 2, 2017.
Posted online 
June 09, 2017
Copyright & Usage 
© 2017. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

Article Versions

  • Previous version (June 9, 2017 - 01:54).
  • You are viewing the most recent version of this article.

Author Information

  1. Ashlee J. Conway1,
  2. Fiona C. Brown1,
  3. Robert O. Fullinfaw2,
  4. Benjamin T. Kile3,
  5. Stephen M. Jane1,4 and
  6. David J. Curtis1,*
  1. 1Australian Centre for Blood Diseases, Monash University and Clinical Haematology, Alfred Health, Melbourne 3004, Australia
  2. 2Porphyria Reference Laboratory, Biochemistry Department, Royal Melbourne Hospital, Parkville 3050, Australia
  3. 3ACRF Chemical Biology Division, The Walter and Eliza Hall Institute of Medical Research, Parkville 3052, Australia
  4. 4Central Clinical School, Monash University, Melbourne 3004, Australia
  1. ↵*Author for correspondence (david.curtis{at}monash.edu)

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Total7561968848

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Keywords

  • Ethyl-N-Nitrosourea
  • Hereditary coproporphyria
  • CPOX
  • Anaemia

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RESEARCH ARTICLE
A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
Ashlee J. Conway, Fiona C. Brown, Robert O. Fullinfaw, Benjamin T. Kile, Stephen M. Jane, David J. Curtis
Disease Models & Mechanisms 2017 10: 1005-1013; doi: 10.1242/dmm.029116
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RESEARCH ARTICLE
A mouse model of hereditary coproporphyria identified in an ENU mutagenesis screen
Ashlee J. Conway, Fiona C. Brown, Robert O. Fullinfaw, Benjamin T. Kile, Stephen M. Jane, David J. Curtis
Disease Models & Mechanisms 2017 10: 1005-1013; doi: 10.1242/dmm.029116

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