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...

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Main Authors:	Siti Aishah Sulaiman, Nor Azian Abdul Murad, Chow, Yock Ping, Zam Zureena Mohd Rani, Salwati Shuib, Dayang Anita A. Aziz, Hana Azhari, Sharifah Azween Syed Omar, Zarina Abdul Latiff, Rahman Jamal
Format:	Article
Language:	en
Published:	Pusat Perubatan Universiti Kebangsaan Malaysia 2018
Online Access:	http://journalarticle.ukm.my/13247/1/39-153-1-PB.pdf http://journalarticle.ukm.my/13247/ http://spaj.ukm.my/apjmm/index.php/apjmm/issue/view/19
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