Screening of three Mediterranean phenylketonuria mutations in Tunisian families-Reference-Cited by-同舟云学术

Screening of three Mediterranean phenylketonuria mutations in Tunisian families

Published:2012-04 Issue:1 Volume:91 Page:91-94
ISSN:0022-1333
Container-title:Journal of Genetics
language:en
Short-container-title:J Genet

Author:

KHEMIR SAMEH,SIALA HAJER,TAIEB SAMEH HADJ,CHERIF WAFA,AZZOUZ HATEM,KÉFI RYM,ABDELHAK SONIA,KHOUJA NAZIHA,TEBIB NEJI,MASSAOUD TAIEB,DRIDI MARIE FRANÇOISE BEN,KAABACHI NAZIHA

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://link.springer.com/content/pdf/10.1007/s12041-012-0140-z.pdf

Reference16 articles.

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2. Berthelon M., Caillaud C., Rey F., Labrune P., Melle D., Feingold J. et al. 1991 Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus. Hum. Genet. 86, 355–358.

3. Dahri S., Desviat L. R., Pérez B., Leal F., Ugarte M. and Chabraoui L. 2010 Mutation analysis of phenylketonuria patients from Morocco: High prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X. Clin. Biochem. 43, 76–81.

4. Dianzani I., Giannattasio S., de Sanctis L., Marra E., Ponzone A., Camaschella C. et al. 1994 Genetic history of phenylketonuria mutations in Italy. Am. J. Hum. Genet. 55, 851–853.

5. Dianzani I., Giannattasio G., de Sanctis L., Alliaudi C., Lattanzio P., Dionisi Vici C. et al. 1995 Characterization of phenylketonuria alleles in the Italian population. Eur. J. Hum. Genet. 3, 294–302.

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