DIAGNOSTIC PROBLEMS OF MUCOVISCIDOSIS AND WAYS OF SOLUTION IN RUSSIA

• Glavni autori: A. A. Baranov (Autor), N. I. Kapranov (Autor), N. Yu. Kashirskaya (Autor), L. S. Namazova-Baranova (Autor), V. D. Sherman (Autor), O. I. Simonova (Autor), A. Yu. Tomilova (Autor), K. V. Sevost'yanov (Autor), A. M. Pushkov (Autor), A. L. Vladykin (Autor), N. V. Shatokhin (Autor)
• Format: Knjiga
• Izdano: Union of pediatricians of Russia, 2014-11-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

Mucoviscidosis is a monogenic autosomal recessive caused by the CFTR gene mutations and characterized by pronounced genetic heterogeneity and clinical polymorphism, which emphasizes the need in comprehensive diagnosis and molecular-genetic verification of the final diagnosis. Quality and duration of...