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Possible modifier genes in the variation of neurofibromatosis type 1 clinical phenotypes
(Taylor and Francis Ltd, 2018-04-03)
Neurofibromatosis type 1 (NF1) is the most common neurogenetic disorder worldwide, caused by mutations in the (NF1) gene. Although NF1 is a single-gene disorder with autosomal-dominant inheritance, its clinical expression ...