A new, high frequency variant of α1-antitrypsin
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00284429.pdf
Cited by 20 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Rare variants in alpha 1 antitrypsin deficiency: a systematic literature review;Orphanet Journal of Rare Diseases;2024-02-22
2. Linkage between serum cholinesterase 2 (CHE2) and γ-crystallin gene cluster (CRYG): assignment to chromosome 2;Clinical Genetics;2008-06-28
3. Gentics and linkage relationships of the C3 polymorphism: discovery of C3-Se linkage and assignment of LES-C3-DM-Se-PEPD-Lu synteny to chromosome 19;Clinical Genetics;2008-06-28
4. Pi phenotypes of alpha1-antitrypsin in Southern England: Identification of M subtypes and implications for genetic studies;Clinical Genetics;2008-04-23
5. Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of (?1-antitrypsin);Human Genetics;1986-10
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