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

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Mutation in ribosomal protein L21 underlies hereditary hypotrichosis simplex

Cheng Zhou1, Dongjie Zang, Yan Jin

  • 1Department of Dermatology, Peking University People's Hospital, No. 11 Xizhimen South Street, Beijing, People's Republic of China.

Human Mutation
|March 18, 2011
PubMed

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