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Fig. 4 | Genome Medicine

Fig. 4

From: Exome sequencing in undiagnosed congenital myopathy reveals new genes and refines genes–phenotypes correlations

Fig. 4

Congenital myopathy-causing genes. In total, pathogenic variants in 48 genes have been identified in the MYOCAPTURE cohort. The diagram depicts the distribution of these genes based on histological phenotypes and the intersections between phenotypes. The new genes not previously linked to a congenital myopathy are indicated in bold and underlined. CFTD congenital fiber type disorder, CNM centronuclear myopathy, TAM tubular aggregate myopathy

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Genome Medicine

ISSN: 1756-994X

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