N. Proņina

发表

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

H. Rüffert, T. Kauliņš, N. Proņina, 2008 .

Phenylketonuria in the Latvian population: Molecular basis, phenylalanine levels, and patient compliance

L. Gailīte, M. Kreile, N. Proņina, 2020, Molecular genetics and metabolism reports.

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

N. Proņina, R. Lugovska, 2011 .

The molecular basis of phenylketonuria in Latvia

S. Giannattasio, N. Proņina, P. Lattanzio, 2003, Human mutation.

FMR1 Linked haplotype analysis in a mentally retarded male population

B. Lāce, N. Proņina, Z. Daneberga, 2011 .

Y chromosome—a tool in infertility studies of Latvian population

A. Krūmiņa, L. Pliss, V. Baumanis, 2011, Russian Journal of Genetics.

Mitochondrial DNA Portrait of Latvians: Towards the Understanding of the Genetic Structure of Baltic‐Speaking Populations

R. Villems, K. Tambets, A. Krūmiņa, 2005, Annals of human genetics.

Fragile X Syndrome in Mentally Retarded Patients from Latvia

Z. Krūmiņa, B. Lāce, N. Proņina, 2009 .

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

A. Krūmiņa, S. Kušķe, A. Petersons, 2009 .