Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management.

Diagnostics (Basel) · 2021 · PMC8622093 · PMID 34829490

Europe PMC DOI

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closest p

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quite significantno p-value reported

Even though the number of patients studied is quite significant, research in this area, performed in the clinics and laboratories, is still very important [ 2 ].

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.