Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, o...
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes
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Author / Creator
Stolarova, Lenka , Jelinkova, Sandra , Storchova, Radka , Machackova, Eva , Zemankova, Petra , Vocka, Michal , Kodet, Ondrej , Kral, Jan , Cerna, Marta , Volkova, Zuzana , Janatova, Marketa , Soukupova, Jana , Stranecky, Viktor , Dundr, Pavel , etova, Lenka , Macurek, Libor , Kleiblova, Petra and Kleibl, Zdenek
Publisher
Basel: MDPI AG
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English
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Basel: MDPI AG
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Contents
Cutaneous melanoma is the deadliest skin malignity with a rising prevalence worldwide. Patients carrying germline mutations in melanoma-susceptibility genes face an increased risk of melanoma and other cancers. To assess the spectrum of germline variants, we analyzed 264 Czech melanoma patients indicated for testing due to early melanoma (at <25 ye...
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Full title
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 Genes
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TN_cdi_doaj_primary_oai_doaj_org_article_2465a0fc97634ec4b67bb6e3d6c027fe
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2465a0fc97634ec4b67bb6e3d6c027fe
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ISSN
2227-9059
E-ISSN
2227-9059
DOI
10.3390/biomedicines8100404