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Neurofibromatosis type 1
Summary
General Info
Curated Studies
Most Correlated Studies
OMIM - Congenital disorder
Mouse Phenotypes - Autosomal dominant hereditary disorder
Genome-wide transcriptional profiling of NF1-haploinsufficiency in human: Coriell kindred
Plexiform neurofibroma NF1-deficient ipNF05.5 and ipNF9511.bc cells resistant to TAK-733
Dermal fibroblasts from neurofibroma surrounding tissue with SVEP1 siRNA knockdown
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Pheochromocytoma associated with primary hyperparathyroidism and type 1 neurofibromatosis].
Novel germinal mutation in NF1: case report.
Destabilizing NF1 variants act in a dominant negative manner through neurofibromin dimerization.
The therapeutic potential of neurofibromin signaling pathways and binding partners.
New insights into the molecular basis of spinal neurofibromatosis type 1.
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Neurofibromatosis Type 1 Patient Registry
Spinal Abnormalities in Neurofibromatosis Type 1 (NF1)
Neurofibromatosis Type 1 Brain Tumor Genetic Risk
Analysis of Plasma for Diagnosis and Follow-up of Neurofibromatosis Type 1
Non-invasive Stimulation in Neurofibromatosis Type 1
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