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...
| Main Authors: | , , , , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Pusat Perubatan Universiti Kebangsaan Malaysia
2018
|
| Online Access: | http://journalarticle.ukm.my/13247/ http://journalarticle.ukm.my/13247/ http://journalarticle.ukm.my/13247/1/39-153-1-PB.pdf |