Author:
Shabbeer Junaid,Yasuda Makiko,Luca Edlira,Desnick Robert J
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference24 articles.
1. α-Galactosidase A deficiency: Fabry disease;Desnick,2001
2. Fabry's disease: enzymatic diagnosis of hemizygotes and heterozygotes. α-Galactosidase activities in plasma, serum, urine, and leukocytes;Desnick;J. Lab. Clin. Med.,1973
3. Gene action in the X-chromosome of the mouse (Mus musculus L.);Lyon;Nature,1961
4. X-chromosome inactivation and the diagnosis of X-linked disease in females;Brown;J. Med. Genet.,1993
5. Fabry's disease: normal alpha-galactosidase activity and urinary—sediment glycosphingolipid levels in two obligate heterozygotes;Avila;Br. J. Dermatol.,1973
Cited by
82 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