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Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R. [electronic resource] by
- Hasanoglu, Alev
- Balwani, Manisha
- Kasapkara, Ciğdem S
- Ezgü, Fatih S
- Okur, Ilyas
- Tümer, Leyla
- Cakmak, Alpay
- Nazarenko, Irina
- Yu, Chunli
- Clavero, Sonia
- Bishop, David F
- Desnick, Robert J
Producer: 20110512
In:
Journal of inherited metabolic disease vol. 34
Availability: No items available.
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