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

by Proņina Natālija, Lugovska Rita
Published 2011-01-01

Fragile X Syndrome in Mentally Retarded Patients from Latvia

by Daneberga Zanda, Krūmiņa Zita, Lāce Baiba, Bauze Daiga, Proņina Natālija, Lugovska Rita
Published 2009-01-01

Identification of A Novel Mutation in RYR1 Gene in Malignant Hyperthermia-Like Patient's Family Members

by Kauliñš Tālis, Proñina Natālija, Rüffert Henrik, Wehner Markus, Mihelsons Māris, Osipova Oksana, Miščuks Aleksejs
Published 2008-01-01

Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss

by Šterna Olga, Proņina Natālija, Grīnfelde Ieva, Kušķe Sandra, Krūmiņa Astrīda, Lugovska Rita, Pētersons Aigars
Published 2009-01-01