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Detection of Gene Mutation and Relationship between Phenotype and Genotype in Four Chinese Families with Osteogenesis Imperfecta / 实用儿科临床杂志
Journal of Applied Clinical Pediatrics ; (24)2004.
Article Dans Chinois | WPRIM | ID: wpr-640268
ABSTRACT
T mutation was detected in the 4th propositus at the 9th intron,but any COL1A1 or COL1A2 gene mutation was detected in the third propositus and the other members in the former families.Conclusions The genetic mutation of COL1A1 may result in OI in China,but other mutations may also exist.Moreover,the phenotype was influenced not only by OI genotype,but also by the genetic background,environment and other factors.

Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Type d'étude: Etude diagnostique langue: Chinois Texte intégral: Journal of Applied Clinical Pediatrics Année: 2004 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Type d'étude: Etude diagnostique langue: Chinois Texte intégral: Journal of Applied Clinical Pediatrics Année: 2004 Type: Article