October 11, 2014Journal of Allergy and Clinical ImmunologyOpen Access

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

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Abstract

These studies highlight the need for RAB27A sequencing in patients with FHL with normal pigmentation and identify a critical binding site for Munc13-4 on Rab27a, revealing the molecular basis of this interaction.

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Cite This Study

Cetica et al. (2014) studied this question.

synapsesocial.com/papers/69d80bbc617ce96c42ae298a https://doi.org/10.1016/j.jaci.2014.08.039

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Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

Abstract

Discussion

Cite This Study

Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding

Abstract

Discussion

Cite This Study

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