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Updated: Jan 23, 2026

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Analyzing the Functions of Mast Cells In Vivo Using 'Mast Cell Knock-in' Mice
Published on: May 27, 2015
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The mast cell - neurofibromatosis connection
D Antonopoulos1,2, I Tsilioni2, N A A Balatsos1
1Department of Biochemistry and Biotechnology, University of Thessaly, Biopolis, Larissa, Greece.
Journal of Biological Regulators and Homeostatic Agents
|June 12, 2019
Summary
Neurofibromatosis type 1 (NF1) is a genetic disorder caused by mutations in the neurofibromin gene. This condition affects about 1 in 3000 people globally and is fully penetrant by age five.
Area of Science:
- Genetics
- Molecular Biology
- Neurology
Background:
- Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder.
- It affects approximately 1 in 3000 individuals worldwide.
- NF1 arises from germline mutations in the neurofibromin gene.
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