HNF4A-related Fanconi syndrome in a Chinese patient: a case report and review of the literature

Overview of attention for article published in Journal of Medical Case Reports, July 2018

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HNF4A-related Fanconi syndrome in a Chinese patient: a case report and review of the literature. https://t.co/b9Mr0kyNud https://t.co/lcwBuRdsDv

20 Jul 2018

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"This is the first case of HNF4A mutation associated with an auditory phenotype. It expands the clinical phenotypes and supports speculation in the literature that HNF4A may be a candidate gene for deafness." https://t.co/b9Mr0kyNud https://t.co/Fr6yibkl7w

16 Jul 2018

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HNF4A-related Fanconi syndrome in a Chinese patient: a case report and review of the literature. https://t.co/b9Mr0kQolL

16 Jul 2018

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