Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Samrah I Siddiqui"'
Autor:
Faisal S. Ali, Mohammed R. Gandam, Maryam R. Hussain, Noor Mualla, Samreen Khuwaja, Nivedita Sundararajan, Samrah I. Siddiqui, Syeda Naqvi, Roy Tomas DaVee, Nirav Thosani
Publikováno v:
Surgical Endoscopy.
Publikováno v:
Cureus
Hereditary tyrosinemia type 1 (HT-1) is a rare autosomal recessive disorder caused by a deficiency in the enzyme fumarylacetoacetate hydrolase (FAH), which catalyzes the final step in the tyrosine degradation pathway. Hereditary tyrosinemia is a hete
Autor:
Tomas DaVee, Syeda Naqvi, Nirav Thosani, Srinivas Ramireddy, Nivedita Sundararajan, Shahrooz Rashtak, Ricardo Badillo, Samrah I. Siddiqui, Faisal Ali, Sushovan Guha, Maryam R. Hussain, Samreen Khuwaja, Mohammed Gandam
Publikováno v:
Gastrointestinal Endoscopy. 93:AB79-AB80