Search Results - Preetha Remesh

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    Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: a case report by Joshi Stephen, Sheela Nampoothiri, K. P. Vinayan, Dhanya Yesodharan, Preetha Remesh, William A. Gahl, May Christine V. Malicdan

    Published 2018
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