Exome sequencing identifies a novel frameshift variant causing hypomagnesemia with secondary hypocalcemia

Overview of attention for article published in CEN Case Reports, August 2018

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Novel TRPM6 frameshift variant https://t.co/JEgcmJb6UB causing #hypomagnesemia identified in #Pakistani #patient via #exome #sequencing https://t.co/0bbvfPOEIP

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Exome sequencing identifies a novel frameshift variant causing hypomagnesemia with secondary hypocalcemia. https://t.co/eqByzVMLCm

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