Evidence for the Presence of the Second Allele of the Neurofibromatosis Type 1 Gene in Melanocytes Derived from Café au Lait Macules of NF1 Patients
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference20 articles.
1. The Neurofibromatoses, a Pathogenetic and Clinical Overview;Huson,1994
2. Mutation and Cancer: Statistical Study of Retinoblastoma
3. Loss ofNF1 alleles in phaeochromocytomas from patients with type 1 neurofibromatosis
4. Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
5. Loss of The Normal NF1 Allele from the Bone Marrow of Children with Type 1 Neurofibromatosis and Malignant Myeloid Disorders
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1. Towards a neurobiological understanding of pain in neurofibromatosis type 1: mechanisms and implications for treatment;Pain;2019-02-05
2. Pigmented (melanotic) diffuse neurofibroma of the back in neurofibromatosis type 1;GMS INTERDISCIP PLAS;2018
3. Independent NF1 mutations underlie café-au-lait macule development in a woman with segmental NF1;Neurology Genetics;2018-07-23
4. Neurofibromin interacts with the cytoplasmic Dynein Heavy Chain 1 in melanosomes of human melanocytes;FEBS Letters;2013-04-10
5. Mosaïcisme pigmentaire;Annales de Dermatologie et de Vénéréologie;2012-08
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