Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

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In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
00:06

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

L A Everett1, B Glaser, J C Beck

  • 1Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

Nature Genetics
|December 17, 1997
PubMed

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