Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis
Arwa Z. Al-Riyami, Achille Iolascon*, Shoaib Al-Zadjali, Immacolata Andolfo, Sahima Al-Mammari, Francesco Manna, Abdul Hakim Al Rawas, May Jean King, Roberta Russo
*المؤلف المقابل لهذا العمل
نتاج البحث: المساهمة في مجلة › Letter › مراجعة النظراء
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اقتباسات
(Scopus)