Mutations in KIF27, GNAS and IFT140 genes in a patient with VACTERL association: a case report

Mutations in KIF27, GNAS and IFT140 genes in a patient with VACTERL association: a case report

VACTERL association is a rare genetic disorder involving at least three of the following congenital malformations: vertebral defects (V), anal atresia (A), cardiac defects (C), trachea-oesophageal fistula with or without oesophageal atresia (TE), renal anomalies (R) and limb abnormalities (L). Until...

Full description

Bibliographic Details
Main Authors: Siti Aishah Sulaiman (Author), Nor Azian Abdul Murad (Author), Chow, Yock Ping (Author), Zam Zureena Mohd Rani (Author), Salwati Shuib (Author), Dayang Anita A. Aziz (Author), Hana Azhari (Author), Sharifah Azween Syed Omar (Author), Zarina Abdul Latiff (Author), Rahman Jamal (Author)
Format: Article
Language:English
Published: Pusat Perubatan Universiti Kebangsaan Malaysia, 2018.
Online Access:Get fulltext

Internet

Get fulltext

Similar Items