Farheen Khan

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1CO-AUTHORS

Crystallography

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Publications (1)

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|Feb 13, 2020

Clinical and Biochemical Features in a Case of Familial Hypocalciuric Hypercalcemia Type 3 with AP2S1 Gene Mutation in Codon Arg15His.

Mohamed Aashiq, Asma Jassim Malallah, Farheen Khan

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Frequent Collaborators

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Mohamed Aashiq

Frequent Collaborators

1 joint publications

Mohamed Aashiq