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Manal Al-Shawi
Manal Al-Shawi
EIF2AK3
Internal medicine
Wolcott–Rallison syndrome
Mutation
Diabetes mellitus
2
Papers
9
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A unique genotype of pseudohypoaldosteronism type 1b in a highly consanguineous population
2021
Journal of the Endocrine Society
Ali S. Alzahrani
Meshael Alswailem
Bassam Bin Abbas
Ebtesam Qasem
Afaf Alsagheir
Azza Al Shidhani
Aisha Al-Sinani
Maryam Al Badi
Ali Al Maqbali
Manal Al-Shawi
Abdulhameed Albunyan
Abdulghani Bin Nafisah
Yufei Shi
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Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation.
2013
Journal of Pediatric Endocrinology and Metabolism
Manal Al-Shawi
Angham Al Mutair
Sian Ellard
Abdelhadi M. Habeb
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Citations (9)
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