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Journals
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.
Volume 65 (2011): Issue 3-4 (August 2011)
Open Access
Association between minihaplotypes and mutations at the phenylalanine hydroxylase locus in Latvian phenylketonuria patients
Natālija Proņina
Natālija Proņina
and
Rita Lugovska
Rita Lugovska
| Feb 15, 2012
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.
Volume 65 (2011): Issue 3-4 (August 2011)
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Published Online:
Feb 15, 2012
Page range:
73 - 79
DOI:
https://doi.org/10.2478/v10046-011-0021-5
Keywords
phenylalanine hydroxylase
,
phenylketonuria
,
minihaplotype
,
mutation
,
genetic heterogeneity
,
gene
This content is open access.