Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome-Reference-Cited by-同舟云学术

Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndrome

Author:

Ulrich Maximilian¹^ORCID,Tinschert Sigrid²³,Siebert Eberhard⁴,Franke Ingolf⁵,Tüting Thomas⁵,Ulrich Jens⁶,Schanze Denny¹,Wieland Ilse¹,Zenker Martin¹

Affiliation:

1. Institute of Human Genetics University Hospital Otto‐von‐Guericke‐University Magdeburg Germany

2. Medical Faculty Carl Gustav Carus Technical University of Dresden Dresden Germany

3. Division of Human Genetics Medical University of Innsbruck Innsbruck Austria

4. Institute of Neuroradiology Charité Centrum Berlin Germany

5. Department of Dermatology University Hospital Magdeburg Magdeburg Germany

6. Klinik für Dermatologie und Venerologie Harzklinikum Dorothea Christiane Erxleben Quedlinburg Germany

Funder

Novartis

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

Link

Reference16 articles.

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