Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations-Reference-Cited by-同舟云学术

Melanoma cases demonstrate increased carrier frequency of phenylketonuria/hyperphenylalanemia mutations

Author:

Arbesman Joshua¹^ORCID,Ravichandran Sairekha¹,Funchain Pauline²,Thompson Cheryl L.³

Affiliation:

1. Department of Dermatology; Case Western Reserve University; Cleveland OH USA

2. Department of Hematology/Oncology; Cleveland Clinic Foundation; Cleveland OH USA

3. Department of Nutrition; Case Western Reserve University; Cleveland OH USA

Funder

National Institutes of Health

Dermatology Foundation

Fowler Family Foundation

National Human Genome Research Institute

Broad Institute

Yale SPORE in Skin Cancer

National Cancer Institute

Melanoma Research Alliance

Gilead Sciences

Howard Hughes Medical Institute

Department of Dermatology

Yale Comprehensive Cancer Center

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

Link

Reference16 articles.

1. Human gene mutations;Froster;Human Genetics,2001

4. Newborn screening 50 years later: Access issues faced by adults with PKU;Berry;Genetics in Medicine: Official Journal of the American College of Medical Genetics,2013

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