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A Rare Cause of Familial Hypomagnesemia: A Case with Trpm6 Mutation
A Rare Cause of Familial Hypomagnesemia: A Case with Trpm6 Mutation
2021
Merve Sakar
Semra Çetinkaya
Kücukali Gülin Karacan
Şervan Özalkak
Selin Elmao gbreve
ullar imath
Şahin Nursel Murato gbreve
Lu
Melikşah Keskin
Naz Guleray Lafc imath
Erdeve Senay Savas
Keywords:
Hypomagnesemia
Genetics
Mutation (genetic algorithm)
TRPM6
Medicine
Correction
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