Condition: FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6


rs387906807 in MYO1E gene and FOCAL SEGMENTAL GLOMERULOSCLEROSIS 6 PMID 21756023 2011 MYO1E mutations and childhood familial focal segmental glomerulosclerosis.

PMID 21697813 2011 Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome.