Work

Correction: DPH1 syndrome: two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients

Year: 2019

Type: erratum

Source: European Journal of Human Genetics

DOI: 10.1038/s41431-019-0394-5

Authors: Roser Urreizti, Klaus Mayer, Gilad D. Evrony, Edith Said, Laura Castilla-Vallmanya, Neal A. L. Cody, Guillem Plasencia, Bruce D. Gelb, Daniel Grinberg, Ulrich Brinkmann, Bryn D. Webb, Susanna Balcells

Institutions: Centre for Biomedical Network Research on Rare Diseases, Institut de Recerca Sant Joan de Déu, Institut de Biomedicina de la Universitat de Barcelona, Universitat de Barcelona, NYU Langone Health, New York University, University of Malta, Mater Dei Hospital, Sema4 (United States), Icahn School of Medicine at Mount Sinai

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

OpenAlex ID: W4250877776

Cites:

Cited by: 3

Related to: 10