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The Journal of Clinical Investigation|December 18, 2003

Renal Ca2+ wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5Joost G J Hoenderop, Johannes P T M van Leeuwen, Bram C J van der Eerden, et al.

The Journal of Investigative Dermatology|February 22, 2023

CYSRT1: An Antimicrobial Epidermal Protein that Can Interact with Late Cornified Envelope ProteinsHanna Niehues, Gijs Rikken, Ferry F J Kersten, et al.

Human Mutation|June 6, 2006

Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing lossErsan Kalay, Yun Li, Abdullah Uzumcu, et al.

Nature Genetics|June 5, 2007

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Moin D Mohamed, et al.

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Showing results (11-20 of 14) with videos related to

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Pageof 2

You have reached the last page of results.This site can display upto 14 results.

The Journal of Clinical Investigation|December 18, 2003

Renal Ca2+ wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5Joost G J Hoenderop, Johannes P T M van Leeuwen, Bram C J van der Eerden, et al.

The Journal of Investigative Dermatology|February 22, 2023

CYSRT1: An Antimicrobial Epidermal Protein that Can Interact with Late Cornified Envelope ProteinsHanna Niehues, Gijs Rikken, Ferry F J Kersten, et al.

Human Mutation|June 6, 2006

Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing lossErsan Kalay, Yun Li, Abdullah Uzumcu, et al.

Nature Genetics|June 5, 2007

Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosisAnneke I den Hollander, Robert K Koenekoop, Moin D Mohamed, et al.

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