NovelIFT122mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum-Reference-Cited by-同舟云学术

NovelIFT122mutations in three Argentinian patients with cranioectodermal dysplasia: Expanding the mutational spectrum

Author:

Moosa Shahida¹²³,Obregon Maria Gabriela⁴,Altmüller Janine²⁵,Thiele Holger⁵,Nürnberg Peter³⁵⁶,Fano Virginia⁷,Wollnik Bernd¹²³

Affiliation:

1. Institute of Human Genetics; University Medical Center Göttingen; Göttingen Germany

2. Institute of Human Genetics; University of Cologne; Cologne Germany

3. Center for Molecular Medicine Cologne (CMMC); University of Cologne; Cologne Germany

4. Department of Medical Genetics; Garrahan Pediatrics Hospital; Buenos Aires Argentina

5. Cologne Center for Genomics (CCG); University of Cologne; Cologne Germany

6. Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD); University of Cologne; Cologne Germany

7. Department of Growth and Development; Garrahan Pediatrics Hospital; Buenos Aires Argentina

Funder

German Federal Ministry of Education and Research (BMBF)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference10 articles.

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