...NF1) is the most common neurogenetic disorder worldwide, caused by mutations in the (NF1) gene. Although NF1 is a single...
...NF1 patients and future directions. MEK inhibitors have demonstrated efficacy for NF1-related conditions, including plex...
...NF1 deletion. To study the extent of the microdeletion in these NF1 patients, we generated a partial physical map of the...
...NF1 gene was isolated in 1991, our understanding of the genetics of NF1 has increased remarkably. One of the most striki...
...Nf1 mutants. Mechanistically, we demonstrate that HCN1 is a novel NF1-interacting protein for which loss of NF1 results ...
...NF1) is a genetic disease caused by mutations in Neurofibromin 1 (NF1). NF1 patients present with a variety of clinical ...
...NF1 deletions but may also occur in individuals with type-2 NF1 deletions. Our findings support the concept of an NF1 mi...
...Nf1 function (Nf1+/- mice), and a second with somatic biallelic Nf1 inactivation in neuroglial progenitor cells (Nf1GFAP...
...NF1 without genetic study, individuals with NF1 germline variants with or without clinical NF1 or associated with somati...
...NF1 coding regions (Marchuk et al., 1992). Fluorescence in situ hybridization (FISH) using these clones has identified N...
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