DOENÇA DE TAY-SACHS - Genética - ufcspa

BIBLIOGRAFIA
1)Scriver CR, Blandet AL, Sey WS, Valle D (eds). The metabolic and molecular bases of
inherited disease, 7ª edição. Editora Mac Graw-Hill, 1995.
2)Emery AEH, Rimon’s DL (eds). Principals and Practice of Medical Genetics, Volume
II, 3ª edição. Edingurg , London, Madrid, Melbourne, San Fransisco, Tokyo, Editora
Churchill Livinstone, 1996.
3) Mahuran DJ. Biochemical consequences of mutations causing the GM2 gangliosidoses.
Biochimica et Biophysica Acta 1455, 105-138, 1999.
4)Mc Kusich VA (ed). Mendelian inherited in man – a catalog of human genes and
genetic disorders, volume II, 11ª edição. London, The Johns Hopkins University Press,
1994.
5)Gelehrter TD, Collins FS, Ginsburg D (eds). Principal of Medical Genetics, 2ª edição.
Baltimore, Willians & Wilkins, 1998.
6)www.geneclinics.com
7)Rozenberg R, Pereira Ld. The frequency of Tay Sachs disease causing mutations in the
Brazlilian Jewish population justifies a carrier screening program. São Paulo Medical
Journal 119(4):146-9, jul 2001.
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