Genes, Vol. 11, Pages 821: A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in Siblings

In this study, we describe a unique case, in which two siblings with a rare disorder have different pathologic genotypes.

Source: Genes - July 18, 2020 Category: Genetics & Stem Cells Authors: Olga Shchagina Ludmila Bessonova Igor Bychkov Tatiana Beskorovainaya Aleksander Poliakov Tags: Brief Report Source Type: research