Once again, rare diseases provide a spotlight

Mol Genet Metab. 2016 May;118(1):1-2. doi: 10.1016/j.ymgme.2016.03.002. Epub 2016 Mar 5.

Authors

Tamanna Roshan Lal¹, Daniel K Borger¹, Ellen Sidransky²

Affiliations

¹ Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States.
² Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States. Electronic address: sidranse@mail.nih.gov.

No abstract available

Keywords: Gaucher disease; Lysolipids; Monoclonal gammopathy; Multiple myeloma.

Publication types

Research Support, N.I.H., Intramural

MeSH terms

Animals
Diagnosis, Differential
Disease Models, Animal
Gaucher Disease / complications*
Gaucher Disease / metabolism
Humans
Lysophosphatidylcholines / immunology*
Monoclonal Gammopathy of Undetermined Significance / etiology
Monoclonal Gammopathy of Undetermined Significance / immunology
Monoclonal Gammopathy of Undetermined Significance / metabolism*
Multiple Myeloma / etiology
Multiple Myeloma / immunology
Multiple Myeloma / metabolism*
Rare Diseases

Substances

Lysophosphatidylcholines

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