Preliminary screening of Alpha-1 Antitrypsin (A1AT) Phenotype among Healthy Kelantanese

Introduction: Alpha-1 antitrypsin deficiency is a hereditary condition resulting from a SERPINA1 gene mutation that increases susceptibility to emphysema and cirrhosis, thus prompting efforts for early screening. The standard allele is “M,” while the allelic variants most frequently linked to pat...

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Bibliographic Details

Main Authors:	Wan Azman, Wan Norlina, Mohammad Nazri, Nor Amirah, Tuan Ismail, Tuan Salwani, Harun, Azian, Yaacob, Najib Majdi, Sulong, Sarina, Kuttulebbai Naina Mohamed Salam, Sirajudeen, Che Mat, Mahaya, Zulkeflee, Hani Ajrina, Musa, Norsyuhadah
Format:	Article
Language:	en
Published:	Faculty of Medicine Universiti Kebangsaan Malaysia 2023
Subjects:	R Medicine (General)
Online Access:	http://irep.iium.edu.my/109212/7/109212_Preliminary%20screening%20of%20Alpha-1%20Antitrypsin%20%28A1AT%29.pdf http://irep.iium.edu.my/109212/
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