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Autor:
Maia Filho, Josevaldo Monteiro, Medeiros, Luana de Oliveira, Freitas, Abraão Pereira Assis de, Bringel, Ana Camila, Rodrigues, Joyce Maria Malheiro, Lima Filho, Marcos Roberto de Oliveira, Oliveira, Iasmim Chaves de, Ribeiro, Erlane Marques
Publikováno v:
Research, Society and Development; Vol. 11 No. 6; e12811628727
Research, Society and Development; Vol. 11 Núm. 6; e12811628727
Research, Society and Development; v. 11 n. 6; e12811628727
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Research, Society and Development; Vol. 11 Núm. 6; e12811628727
Research, Society and Development; v. 11 n. 6; e12811628727
Research, Society and Development
Universidade Federal de Itajubá (UNIFEI)
instacron:UNIFEI
Achondroplasia is a rare disease of autosomal dominant inheritance, caused by the replacement of the amino acid glycine by arginine at position 380, affecting the fibroblast growth factor 3 receptor (FGRF-3). Its characteristics are evident since int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::d392e9a5a29d411f66fcff5524e4a5a0
https://rsdjournal.org/index.php/rsd/article/view/28727
https://rsdjournal.org/index.php/rsd/article/view/28727
