Mutation of Solute Carrier SLC16A12 Associates with a Syndrome Combining Juvenile Cataract with Microcornea and Renal Glucosuria - Research Collection

Metadata only

Autor(in)

Kloeckener-Gruissem, Barbara

Vandekerckhove, Kristof

Nürnberg, Gudrun

Neidhardt, John

Zeitz, Christina

Nürnberg, Peter

Schipper, Isaak

Berger, Wolfgang

Datum

2008-03

Typ

Journal Article

Zitate

56 Zitate in Web of Science

60 Zitate in Scopus

ETH Bibliographie

yes

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Publikationsstatus

published

Externe Links

https://doi.org/10.1016/j.ajhg.2007.12.013

Zeitschrift / Serie

American Journal of Human Genetics

Band

82(3)

Seiten / Artikelnummer

772 - 779

Verlag

Cell Press

Anmerkungen

Published online 14 February 2008.

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Zitate

56 Zitate in Web of Science

60 Zitate in Scopus

ETH Bibliographie

yes

Altmetrics