Clinical and molecular phenotyping of a child with Hermansky-Pudlak syndrome-7, an uncommon genetic type of HPS

Molecular Genetics and Metabolism - Tập 120 - Trang 378-383 - 2017
Melanie M. Bryan1, Nathanial J. Tolman1, Karen L. Simon1, Marjan Huizing1, Robert B. Hufnagel2, Brian P. Brooks2, Vladislav Speransky3, James C. Mullikin4, William A. Gahl1,5,6, May Christine V. Malicdan6, Bernadette R. Gochuico1
1Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA
2Ophthalmic Genetics and Visual Function Branch, National Eye Institute, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA
3National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA
4NIH Intramural Sequencing Center, National Institutes of Health, 5625 Fishers Lane, Rockville, MD 20852, USA
5Office of the Clinical Director, National Human Genome Research Institute, National Institutes of Health, 10 Center Drive, Bethesda, MD 20892, USA
6NIH Undiagnosed Diseases Program, Common Fund, Office of the Director, 9000 Rockville Pike, National Institutes of Health, Bethesda, MD 20892, USA

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