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Mohammed S. Althobaiti
Mohammed S. Althobaiti
Family history
end stage renal disease
Mutation
Medicine
Physical therapy
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Primary hyperoxaluria Type 1: A case report in an extended family with a novel AGXT gene mutation.
2020
Medicine
Mohamed W. Abukhatwah
Samia H. Almalki
Mohammed S. Althobaiti
Abdulla O. Alharbi
Najla K Almalki
Naglaa M. Kamal
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