The Molecular Anatomy of Spontaneous Germline Mutations in Human Testes

The frequency of the most common sporadic Apert syndrome mutation (C755G) in the human fibroblast growth factor receptor 2 gene (FGFR2) is 100–1,000 times higher than expected from average nucleotide substitution rates based on evolutionary studies and the incidence of human genetic diseases. To det...

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Detalles Bibliográficos
Autores principales: Qin, Jian, Calabrese, Peter, Tiemann-Boege, Irene, Shinde, Deepali Narendra, Yoon, Song-Ro, Gelfand, David, Bauer, Keith, Arnheim, Norman
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2007
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1951783/
https://www.ncbi.nlm.nih.gov/pubmed/17760502
http://dx.doi.org/10.1371/journal.pbio.0050224

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1951783/
https://www.ncbi.nlm.nih.gov/pubmed/17760502
http://dx.doi.org/10.1371/journal.pbio.0050224

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