Author:
Rashid Md. Harun-Or,Sadik Golam,Alam AHM Khurshid,Tanaka Toshihisa
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology,Biochemistry
Reference36 articles.
1. Desnick RJ, Schidler D. α-N-acetylgalactosaminidase deficiency: Schindler disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, editors. The metabolic and molecular bases of inherited disease. Eighth ed. New York: McGraw-Hill; 2001. p. 3483–505.
2. Schindler D, Bishop DF, Wolfe DE, Wang AM, Egge H, Lemieux RU, Desnick RJ. Neuroaxonal dystrophy due to lysosmal α-N-acetylgalactosaminidase deficiency. N Engl J Med. 1989;320:1735–40.
3. van Diggelen OP, Schindler D, Kleijer WJ, Huijmans JM, Galjaad H, Linden HU, Peter-Katalinic J, Egge H, Dabrow-ski U, Cantz M. Lysosomal α-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease. Lancet. 1987;2:804.
4. Chabas A, Duque J, Gort L. A new infantile case of alpha-N-acetylgalactosaminidase deficiency. Cardiomyopathy as a presenting symptom. J Inherit Metab Dis. 2007;30:108.
5. Kanzaki T, Yokota M, Mizuno N, Matsumoto Y, Hirabayashi Y. Novel lysosomal glycoaminoacid storage disease with angiokeratoma corporis diffusum. Lancet. 1989;22:875–7.