Characterization of the Molecular Defects in Rab27a, Caused by RAB27A Missense Mutations Found in Patients with Griscelli Syndrome-Reference-Cited by-同舟云学术

Characterization of the Molecular Defects in Rab27a, Caused by RAB27A Missense Mutations Found in Patients with Griscelli Syndrome

Published:2003-03 Issue:13 Volume:278 Page:11386-11392
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Bahadoran Philippe,Busca Roser,Chiaverini Christine,Westbroek Wendy,Lambert Jo,Bille Karine,Valony Gaëlle,Fukuda Mitsunori,Naeyaert Jean-Marie,Ortonne Jean-Paul,Ballotti Robert

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference28 articles.

1. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

2. Griscelli disease maps to chromosome 15q21 and is associated with mutations in the Myosin-Va gene

3. Novel myosin heavy chain encoded by murine dilute coat colour locus

4. Direct interaction of microtubule- and actin-based transport motors

5. Class V myosins

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