A novel, putatively null, FGD1 variant leading to Aarskog-Scott syndrome in a family from UAE

BACKGROUND: The X-linked condition “Aarskog-Scott syndrome (AAS)” causes a characteristic combination of short stature, facial, genital and skeletal anomalies. Studies elucidated a causative link between AAS and mutations in the FGD1 gene, which encodes a Rho/Rac guanine exchange factor. FGD1 is inv...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:BMC Pediatr
Hlavní autoři: Hamzeh, Abdul Rezzak, Saif, Fatima, Nair, Pratibha, Binjab, Asma Jassim, Mohamed, Madiha, Al-Ali, Mahmoud Taleb, Bastaki, Fatma
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2017
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5248450/
https://ncbi.nlm.nih.gov/pubmed/28103835
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-017-0781-4
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky