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Association between minihaplotypes and mutations at the phenylalanine hydroxylase locus in Latvian phenylketonuria patients Cover

Association between minihaplotypes and mutations at the phenylalanine hydroxylase locus in Latvian phenylketonuria patients

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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Open Access
|Feb 2012
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DOI: https://doi.org/10.2478/v10046-011-0021-5 | Journal eISSN: 2255-890X (formerly 1407-009X) | Journal ISSN: 1407-009X
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Language: English
Page range: 73 - 79
Published on: Feb 15, 2012
Published by: Latvian Academy of Sciences
In partnership with: Paradigm Publishing Services
Keywords:
phenylalanine hydroxylase,
phenylketonuria,
minihaplotype,
mutation,
genetic heterogeneity,
PAH gene
Related subjects:
Mathematics,
General mathematics

© 2012 Natālija Proņina, Rita Lugovska, published by Latvian Academy of Sciences
This work is licensed under the Creative Commons License.

Volume 65 (2011): Issue 3-4 (August 2011)
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