Clinical, Molecular, and Cell Biological Aspects of Chediak–Higashi Syndrome
- 31 October 1999
- journal article
- review article
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 68 (2), 283-303
- https://doi.org/10.1006/mgme.1999.2927
Abstract
No abstract availableKeywords
This publication has 127 references indexed in Scilit:
- A novel adaptor-related protein complex.The Journal of cell biology, 1996
- HEAT repeats in the Huntington's disease proteinNature Genetics, 1995
- Interaction of Tyrosine-Based Sorting Signals with Clathrin-Associated ProteinsScience, 1995
- Partial albinism with immunodeficiency (Griscelli syndrome)The Journal of Pediatrics, 1994
- The ancient regulatory-protein family of WD-repeat proteinsNature, 1994
- Complementation analysis of Chediak-Higashi Syndrome: The same gene may be responsible for the defect in all patients and speciesSomatic Cell and Molecular Genetics, 1993
- .alpha.- And .beta.-forms of the 65-kDa subunit of protein phosphatase 2A have a similar 39 amino acid repeating structureBiochemistry, 1990
- Chediak-Higashi gene in humans. II. The selectivity of the defect in natural- killer and antibody-dependent cell-mediated cytotoxicity functionThe Journal of Experimental Medicine, 1980
- Chediak-Higashi gene in humans. I. Impairment of natural - killer functionThe Journal of Experimental Medicine, 1980
- A Human Pigmentary Dilution Based on a Heritable Subcellular Structural Defect—The Chediak-Higashi Syndrome**From the Departments of Pediatrics and Dermatology, University of Minnesota, Minneapolis.Journal of Investigative Dermatology, 1968