Abstract
Understanding the Interactions between the Proteins Implicated in Legius Syndrome and Neurofibromatosis Type 1♦: Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1
Highlights
Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1
Individuals have multiple cafe-au-lait spots that are darker than the surrounding area
Mutations in the SPRED1 gene have been implicated in Legius syndrome
Summary
Interaction between a Domain of the Negative Regulator of the Ras-ERK Pathway, SPRED1 Protein, and the GTPase-activating Protein-related Domain of Neurofibromin Is Implicated in Legius Syndrome and Neurofibromatosis Type 1. Implicated in Legius Syndrome and Neurofibromatosis Type 1ࡗ
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