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Volumn 102, Issue 1, 2011, Pages 29-32

Mutation spectrum of phenylketonuria in Iranian population

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

EID: 78650890341     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2010.09.001     Document Type: Article
Times cited : (44)

References (22)
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    • Phenylketonuria in Iranian population: a study in institutions for mentally retarded in Isfahan
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    • Dworniczak B., Aulehla-Scholz C., Kalaydjieva L., Bartholome K., Grudda K., Horst J. Aberrant splicing of phenylalanine hydroxylase mRNA: the major cause for phenylketonuria in parts of southern Europe. Genomics. 1991, 11:242-246.
    • (1991) Genomics. , vol.11 , pp. 242-246
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    • Analysis of the phenylalanine hydroxylase gene in the Spanish population: mutation profile and association with intragenic polymorphic markers
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.