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Nucleotide sequence of the human alpha-galactosidase A gene.
Division of Medical and Molecular Genetics, Mount Sinai School of Medicine, New York, NY 10029.
PMID: 2542896 [PubMed - indexed for MEDLINE]
PMCID: PMC317741
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Cited by 14 PubMed Central articles
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Effects of a chemical chaperone on genetic mutations in alpha-galactosidase A in Korean patients with Fabry disease.
Park JY, Kim GH, Kim SS, Ko JM, Lee JJ, Yoo HW.
Exp Mol Med. 2009 Jan 31; 41(1):1-7.
[Exp Mol Med. 2009]
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Short-term efficacy of enzyme replacement therapy in Korean patients with Fabry disease.
Choi JH, Cho YM, Suh KS, Yoon HR, Kim GH, Kim SS, Ko JM, Lee JH, Park YS, Yoo HW.
J Korean Med Sci. 2008 Apr; 23(2):243-50.
[J Korean Med Sci. 2008]
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SSCP analysis of paraffin wax embedded tissues in a family with an atypical form of Fabry disease.
Madsen KM, Hasholt L, Berger J, Sørensen SA.
Clin Mol Pathol. 1996 Oct; 49(5):M310-M312.
[Clin Mol Pathol. 1996]
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