Identification of a novel PAX6 mutation in a sporadic case with congenital aniridia / 中华医学遗传学杂志
Chinese Journal of Medical Genetics
;
(6): 616-619, 2019.
Article
Dans Chinois
| WPRIM
| ID: wpr-771954
ABSTRACT
OBJECTIVE@#To identify mutation of the PAX6 gene in a patient with congenital aniridia.@*METHODS@#DNA was extracted from peripheral blood sample of the patient and analyzed by direct PCR-Sanger sequencing.@*RESULTS@#The proband was found to harbor a heterozygous c.239T>A (p.Ile80Asn) mutation of the PAX6 gene. The same mutation was not found in his parents and 150 healthy controls.@*CONCLUSION@#A novel mutation of the PAX6 gene has been identified in a sporadic case with congenital aniridia.
Texte intégral:
Disponible
Indice:
WPRIM (Pacifique occidental)
Sujet Principal:
Pedigree
/
Séquence nucléotidique
/
Aniridie
/
Facteur de transcription PAX6
/
Génétique
/
Mutation
Type d'étude:
Etude diagnostique
/
Étude pronostique
Limites du sujet:
Humains
langue:
Chinois
Texte intégral:
Chinese Journal of Medical Genetics
Année:
2019
Type:
Article
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