The neurofibromatosis type 2 (that abrogate merlins functional activity are located in about 40% of MMs, indicating the need for inactivation in MM development and progression. gene. Because it was demonstrated a homozygous mutation in the gene of mice causes embryonic loss of life by day time 6.5 of their advancement [9], the part of… Continue reading The neurofibromatosis type 2 (that abrogate merlins functional activity are located