Expanding the MYCN Variant Spectrum in Feingold Syndrome Type 1: A Novel N-Terminal Missense Variant Segregating in an Affected Family.
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| Title: | Expanding the MYCN Variant Spectrum in Feingold Syndrome Type 1: A Novel N-Terminal Missense Variant Segregating in an Affected Family. |
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| Authors: | Javier Mérida De la Torre F; Genetics Laboratory, Hospital Regional Universitario, 29011 Málaga, Spain., Porta Pelayo J; Genologica by Health in Code, 29016 Málaga, Spain., Ortiz-Martín I; Genologica by Health in Code, 29016 Málaga, Spain. |
| Source: | Genes [Genes (Basel)] 2026 May 05; Vol. 17 (5). Date of Electronic Publication: 2026 May 05. |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| ISSN: | 2073-4425 |
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| DOI: | 10.3390/genes17050552 |
