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Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria. [electronic resource] by
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Experimental dermatology vol. 14
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Experimental hematology vol. 36
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Sequence variants in nine different genes underlying rare skin disorders in 10 consanguineous families. [electronic resource] by
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- Ahmad, Farooq
- Ansar, Muhammad
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Producer: 20180706
In:
International journal of dermatology vol. 56
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