| 1 | ASAH1, FLGD
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| Atypical presentation of infantile-onset farber disease with novel ASAH1 mutations.
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| Kim SY, Choi SA, Lee S, Lee JS, Hong CR, Lim BC, Kang HJ, Kim KJ, Park SH, Choi M, Chae JH.
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| Am J Med Genet A 170(11):3023-3027. doi: 10.1002/ajmg.a.37846. Epub 2016 Jul 13.
2016
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| 2 | ASAH1, FLGD
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| Molecular analysis of acid ceramidase deficiency in patients with Farber disease.
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| BŠr J, Linke T, Ferlinz K, Neumann U, Schuchman EH, Sandhoff K.
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| Hum Mutat 17 : 199-209. 2001
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| 3 | ASAH1, FLGD
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| Human acid ceramidase gene: novel mutations in farber disease.
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| Zhang Z, Mandal AK, Mital A, Popescu N, Zimonjic D, Moser A, Moser H, Mukherjee AB.
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| Mol Genet Metab 70(4):301-9. 2000
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| 4 | ASAH1, FLGD
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| The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expression.
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| Li CM, Park JH, He X, Levy B, Chen F, Arai K, Adler DA, Disteche CM, Koch J, Sandhoff K, Schuchman EH.
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| Genomics 62(2):223-31 1999
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