A Clinical Variant of Neurofibromatosis Type 1: Familial Spinal Neurofibromatosis with a Frameshift Mutation in the NF1 Gene
The American Journal of Human Genetics1998Vol. 62(4), pp. 834–841
Citations Over TimeTop 10% of 1998 papers
Elisabet Ars, H. Kruyer, Antonia Gaona, Pilar Casquero, Jordi Rosell, Vı́ctor Volpini, Eduard Serra, Conxi Lázaro, Xavier Estivill
Related Papers
- → Insights into the pathogenesis of neurofibromatosis 1 vasculopathy(2000)273 cited
- → Review Article : Neurofibromin in the Brain(2002)27 cited
- → Reduced Expression of Neurofibromin in the Soft Tissue Tumours Obtained from Patients with Neurofibromatosis Type 1(1995)17 cited
- [Neurofibromatosis type 1 --Recklinghausen's disease; pathogenesis and clinical symptoms].(2000)
- The R1947X mutation of NF1 causing autosomal dominant neurofibromatosis type 1 in a Chinese family(2008)