المؤلفون: Liat Drucker, Ruth Navon, Jesaiachu Armand Hemli

المصدر: Human Mutation. 10:451-457

مصطلحات موضوعية: Silent mutation, Genetics, Transition (genetics), Tay-Sachs disease, Biology, Gangliosidosis, medicine.disease, HEXA, Molecular biology, Frameshift mutation, Exon, medicine, Allele, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0cf64ed1f7d735db57d7beff86de98ff
https://doi.org/10.1002/(sici)1098-1004(1997)10:6<451::aid-humu6>3.0.co;2-g

المؤلفون: Liat Drucker, Jesaiachu Armand Hemli, Ruth Navon

المصدر: Human Mutation. 10:451-457

مصطلحات موضوعية: Genetics, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::05ba708db1f5c3a2a36bc66c49c635c7
https://doi.org/10.1002/(sici)1098-1004(1997)10:6<451::aid-humu6>3.3.co;2-g