Fragile X Syndrome in Mentally Retarded Patients from Latvia
Daneberga, Zanda, Krūmiņa, Zita, Lāce, Baiba, Bauze, Daiga, Proņina, Natālija, Lugovska, Rita
Association between minihaplotypes and mutations at the phenylalanine hydroxylase locus in Latvian phenylketonuria patients
Proņina, Natālija, Lugovska, Rita
Spectrum and Frequency of the GJB2 Gene Mutations Among Latvian Patients with Prelingual Nonsyndromic Hearing Loss
Šterna, Olga, Proņina, Natālija, Grīnfelde, Ieva, Kušķe, Sandra, Krūmiņa, Astrīda, Lugovska, Rita, Pētersons, Aigars
Identification of A Novel Mutation in RYR1 Gene in Malignant Hyperthermia-Like Patient's Family Members
Kauliñš, Tālis, Proñina, Natālija, Rüffert, Henrik, Wehner, Markus, Mihelsons, Māris, Osipova, Oksana, Miščuks, Aleksejs