Clinical and functional characterization of two novel ZBTB20 mutations causing Primrose syndrome - Research Collection

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Author

Stellacci, Emilia

Steindl, Katharina

Mercurio, Laura

Anselmi, Massimiliano

Cecchetti, Serena

Hackenberg, Annette

Bocchinfuso, Gianfranco

Bocchinfuso, Gianfranco

Stella, Lorenzo

Tartaglia, Marco

Date

2018-07

Type

Journal Article

Citations

Cited 9 times in Web of Science

ETH Bibliography

yes

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Publication status

published

External links

https://doi.org/10.1002/humu.23546

Journal / series

Human Mutation

Volume

39(7)

Pages / Article No.

959 - 964

Publisher

Wiley-Blackwell

Subject

3q13.31 microdeletion syndrome; functional analyses; mutation spectrum; Primrose syndrome; ZBTB20

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Show all metadata

Citations

Cited 9 times in Web of Science

ETH Bibliography

yes

Altmetrics