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

N. A. Barashkov; L. S. Vychuzhina; A. V. Solovyev; F. M. Teryutin; V. G. Pshennikova; T. E. Burtseva; M. I. Tomsky; F. A. Platonov; G. P. Romanov; N. N. Gotovtsev; E. K. Khusnutdinova; O. L. Posukh; S. A. Fedororva

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

N. A. Barashkov, L. S. Vychuzhina, A. V. Solovyev, F. M. Teryutin, V. G. Pshennikova, T. E. Burtseva, M. I. Tomsky, F. A. Platonov, G. P. Romanov, N. N. Gotovtsev, E. K. Khusnutdinova, O. L. Posukh, S. A. Fedororva

Результат исследования: Научные публикации в периодических изданиях › тезисы › рецензирование

Язык оригинала	английский
Страницы (с-по)	1220-1221
Число страниц	2
Журнал	European journal of human genetics
Том	27
Состояние	Опубликовано - окт. 2019
Событие	52nd Conference of the European-Society-of-Human-Genetics (ESHG) - Gothenburg, Швеция Продолжительность: 15 июн. 2019 → 18 июн. 2019

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Цитировать

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.

@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",

}

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.

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.

Результат исследования: Научные публикации в периодических изданиях › тезисы › рецензирование

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 -