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Search Results - Elnaggari, Mohamed A.
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dRTA and hemolytic anemia: first detailed description of SLC4A1 A858D mutation in homozygous state
by
Fawaz, Naglaa A.
,
Beshlawi, Ismail O.
,
Al Zadjali, Shoaib
,
Al Ghaithi, Hamed K.
,
Elnaggari, Mohamed A.
,
Elnour, Ibtisam
,
Wali, Yasser A.
,
Al-Said, Bushra B.
,
Rehman, Jalil U.
,
Pathare, Anil V.
,
Knox-Macaulay, Huxley
,
Alkindi, Salam S.
Published in
European journal of haematology
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European Journal Of Haematology
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Subjects
Acanthocytosis
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Acidosis, Renal Tubular - Genetics
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Anemia, Hemolytic - Genetics
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Anion Exchange Protein 1, Erythrocyte - Genetics
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Band 3
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Child, Preschool
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Cytoskeleton - Metabolism
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Dna Mutational Analysis
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Drta
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Eae1
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Female
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Hematology
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Hereditary
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Homozygote
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Humans
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Infant
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Kae1
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Life Sciences & Biomedicine
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Male
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Mutation
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Wiley-Blackwell Journals (Backfile Content)
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Wiley-Blackwell Journals
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Wiley-Blackwell Read & Publish Collection
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