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المؤلفون: Betiana G Comas, Sergio Alejandro Rodríguez-Quiroga, Luca Marsili, Josefina Perez-Maturo, Walter Silva, Valeria Salinas, Nerina Martínez, Hernán Amartino, Patricia Vega, Clarisa Maxit, Marcelo Andrés Kauffman, Kevin R Duque, Nancy Medina, Lucia Zavala, Ignacio Sfaello, Alberto J. Espay, Damián Consalvo, Andrea Sturchio, Barbara Grimberg, Dolores González-Morón
المصدر: American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184:876-884
مصطلحات موضوعية: Genetics, Genetic heterogeneity, High-Throughput Nucleotide Sequencing, Biology, Pathogenicity, DNA sequencing, Germline, Clinical neurology, Gene panel, Exome Sequencing, Humans, Uncertain significance, Genetics (clinical), Exome sequencing
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea3a264e8ff7f53b35a965ec3ae51fe7
https://doi.org/10.1002/ajmg.c.31848