Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria.
- DOI
- 10.1086/320118
- Published
- 2001 May
- Container
- American journal of human genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1086/320118,
title = {Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria.},
author = {Lamoril J and Puy H and Whatley SD and Martin C and Woolf JR and Da Silva V and Deybach JC and Elder GH},
year = {2001},
journal = {American journal of human genetics},
doi = {10.1086/320118},
url = {https://doi.org/10.1086/320118}
}RIS
TY - JOUR TI - Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria. AU - Lamoril J AU - Puy H AU - Whatley SD AU - Martin C AU - Woolf JR AU - Da Silva V AU - Deybach JC AU - Elder GH PY - 2001 JO - American journal of human genetics DO - 10.1086/320118 UR - https://doi.org/10.1086/320118 ER -
APA
J, L., H, P., SD, W., C, M., JR, W., V, D. S., JC, D., & GH, E. (2001). Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria.. American journal of human genetics. https://doi.org/10.1086/320118
Source records
- pubmed · retrieved 2026-09-24T23:34:42.394Z