High prevalence of Netherton syndrome in Latvian population caused by founder SPINK5 variant

I Nartisa; L Ozola; I Grantina; G Taurina; R Insberga; L Gailite; N Kurjane

High prevalence of Netherton syndrome in Latvian population caused by founder SPINK5 variant

I Nartisa, L Ozola, I Grantina, G Taurina, R Insberga, L Gailite, N Kurjane

Rīga Stradiņš University

Research output: Contribution to journal › Meeting Abstract › peer-review

Original language	English
Pages (from-to)	441
Number of pages	1
Journal	European Journal of Human Genetics
Volume	31
Issue number	Suppl.1
Publication status	Published - 11 May 2023
Event	55th European-Society-of-Human-Genetics (ESHG) Conference - Hybrid Conference, Vienna, Austria Duration: 11 May 2022 → 14 May 2022 Conference number: 55 https://2022.eshg.org

Field of Science*

3.2 Clinical medicine
3.1 Basic medicine
3.3 Health sciences

Publication Type*

3.3. Publications in conference proceedings indexed in Web of Science and/or Scopus database

Cite this

@article{602caa6ede194eb68951be4b4d595682,

title = "High prevalence of Netherton syndrome in Latvian population caused by founder SPINK5 variant",

author = "I Nartisa and L Ozola and I Grantina and G Taurina and R Insberga and L Gailite and N Kurjane",

year = "2023",

month = may,

day = "11",

language = "English",

volume = "31",

pages = "441",

journal = "European Journal of Human Genetics",

issn = "1018-4813",

publisher = "Nature Publishing Group",

number = "Suppl.1",

note = "55th European-Society-of-Human-Genetics (ESHG) Conference, ESHG ; Conference date: 11-05-2022 Through 14-05-2022",

url = "https://2022.eshg.org",

}

TY - JOUR

T1 - High prevalence of Netherton syndrome in Latvian population caused by founder SPINK5 variant

AU - Nartisa, I

AU - Ozola, L

AU - Grantina, I

AU - Taurina, G

AU - Insberga, R

AU - Gailite, L

AU - Kurjane, N

N1 - Conference code: 55

PY - 2023/5/11

Y1 - 2023/5/11

UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=rsu_pure_&SrcAuth=WosAPI&KeyUT=WOS:001050507001426&DestLinkType=FullRecord&DestApp=WOS

M3 - Meeting Abstract

SN - 1018-4813

VL - 31

SP - 441

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - Suppl.1

T2 - 55th European-Society-of-Human-Genetics (ESHG) Conference

Y2 - 11 May 2022 through 14 May 2022

ER -

High prevalence of Netherton syndrome in Latvian population caused by founder SPINK5 variant

Field of Science*

Publication Type*

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Cite this