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Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia. / Barashkov, N. A.; Vychuzhina, L. S.; Solovyev, A. V. и др.

в: European journal of human genetics, Том 27, 10.2019, стр. 1220-1221.

Результаты исследований: Научные публикации в периодических изданиях › тезисы › Рецензирование

Harvard

Barashkov, NA, Vychuzhina, LS, Solovyev, AV, Teryutin, FM, Pshennikova, VG, Burtseva, TE, Tomsky, MI, Platonov, FA, Romanov, GP, Gotovtsev, NN, Khusnutdinova, EK, Posukh, OL & Fedororva, SA 2019, 'Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia', European journal of human genetics, Том. 27, стр. 1220-1221.

APA

Barashkov, N. A., Vychuzhina, L. S., Solovyev, A. V., Teryutin, F. M., Pshennikova, V. G., Burtseva, T. E., Tomsky, M. I., Platonov, F. A., Romanov, G. P., Gotovtsev, N. N., Khusnutdinova, E. K., Posukh, O. L., & Fedororva, S. A. (2019). Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia. European journal of human genetics, 27, 1220-1221.

Vancouver

Barashkov NA, Vychuzhina LS, Solovyev AV, Teryutin FM, Pshennikova VG, Burtseva TE и др. Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia. European journal of human genetics. 2019 окт.;27:1220-1221.

Author

Barashkov, N. A. ; Vychuzhina, L. S. ; Solovyev, A. V. и др. / Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia. в: European journal of human genetics. 2019 ; Том 27. стр. 1220-1221.

BibTeX

@article{b33af7b6f3314d18b5b544cf948e477c,
title = "Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia",
author = "Barashkov, {N. A.} and Vychuzhina, {L. S.} and Solovyev, {A. V.} and Teryutin, {F. M.} and Pshennikova, {V. G.} and Burtseva, {T. E.} and Tomsky, {M. I.} and Platonov, {F. A.} and Romanov, {G. P.} and Gotovtsev, {N. N.} and Khusnutdinova, {E. K.} and Posukh, {O. L.} and Fedororva, {S. A.}",
year = "2019",
month = oct,
language = "English",
volume = "27",
pages = "1220--1221",
journal = "European journal of human genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
note = "52nd Conference of the European-Society-of-Human-Genetics (ESHG) ; Conference date: 15-06-2019 Through 18-06-2019",

}

RIS

TY - JOUR

T1 - Founder haplotype bearing mutation c.1621C > T (p.Gln541*) in the FYCO1 gene causing of autosomal recessive cataract (CTRCT18) in the Sakha Republic of Russia

AU - Barashkov, N. A.

AU - Vychuzhina, L. S.

AU - Solovyev, A. V.

AU - Teryutin, F. M.

AU - Pshennikova, V. G.

AU - Burtseva, T. E.

AU - Tomsky, M. I.

AU - Platonov, F. A.

AU - Romanov, G. P.

AU - Gotovtsev, N. N.

AU - Khusnutdinova, E. K.

AU - Posukh, O. L.

AU - Fedororva, S. A.

PY - 2019/10

Y1 - 2019/10

UR - https://apps.webofknowledge.com/full_record.do?product=WOS&search_mode=GeneralSearch&qid=8&SID=D6rTq4AR6huSB9fIxpd&page=1&doc=1

M3 - Meeting Abstract

VL - 27

SP - 1220

EP - 1221

JO - European journal of human genetics

JF - European journal of human genetics

SN - 1018-4813

T2 - 52nd Conference of the European-Society-of-Human-Genetics (ESHG)

Y2 - 15 June 2019 through 18 June 2019

ER -

ID: 23386635