Researchers work to unravel the complex genetic disease neurofibromatosis type 1
Tuesday, February 2, 2016 - 15:07
in Biology & Nature
From a collection of more than 7,800 unrelated neurofibromatosis type 1 mutations, researchers have aimed at two goals: correlate a particular mutation with the symptoms that will develop as the child grows, and identify the likely mechanism that caused a group of DNA rearrangement mutations.