Publications by authors named "Buthainah Albash"

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Novel PHKG2 mutation causing GSD IX with prominent liver disease: report of three cases and review of literature.
Buthainah Albash, Faiqa Imtiaz, Hamad Al-Zaidan, Hadeel Al-Manea, Mohammed Banemai

Eur J Pediatr· May 2014

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Mutation in MPDZ causes severe congenital hydrocephalus.
Mohammed S Al-Dosari, Mohammed Al-Owain, Maha Tulbah, Wesam Kurdi, Nouran Adly, Buthainah Albash

J Med Genet· January 2013

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