Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry

A J  Cassidy; S V  Brugnatelli; C Ayuso; A Avila-Fernandez; D Zeller; Douglas H. Lester; The Tayside Centre For Genomic Analysis

Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry

A J Cassidy, S V Brugnatelli, C Ayuso, A Avila-Fernandez, D Zeller, Douglas H. Lester, The Tayside Centre For Genomic Analysis

Research output: Contribution to conference › Poster

Original language	English
Pages	1398
Number of pages	1
Publication status	Published - 2016
Event	American Society of Human Genetics conference 2016 - Vancouver Convention Centre, Vancouver, Canada Duration: 18 Oct 2016 → 22 Oct 2016 http://www.ashg.org/2016meeting/

Conference

Conference	American Society of Human Genetics conference 2016
Abbreviated title	ASHG 2016
Country	Canada
City	Vancouver
Period	18/10/16 → 22/10/16
Internet address	http://www.ashg.org/2016meeting/

Access to Document

http://www.ashg.org/2016meeting/pdf/ASHG2016-posterabstracts.pdf

Cite this

Cassidy, A. J., Brugnatelli, S. V., Ayuso, C., Avila-Fernandez, A., Zeller, D., Lester, D. H., & The Tayside Centre For Genomic Analysis (2016). Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry. 1398. Poster session presented at American Society of Human Genetics conference 2016, Vancouver, Canada. http://www.ashg.org/2016meeting/pdf/ASHG2016-posterabstracts.pdf

Cassidy, A J ; Brugnatelli, S V ; Ayuso, C ; Avila-Fernandez, A ; Zeller, D ; Lester, Douglas H. ; The Tayside Centre For Genomic Analysis. / Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry. Poster session presented at American Society of Human Genetics conference 2016, Vancouver, Canada.1 p.

@conference{88f362e5f32e4ccaa106899e949def7c,

title = "Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry",

author = "Cassidy, {A J} and Brugnatelli, {S V} and C Ayuso and A Avila-Fernandez and D Zeller and Lester, {Douglas H.} and {The Tayside Centre For Genomic Analysis}",

year = "2016",

language = "English",

pages = "1398",

note = "American Society of Human Genetics conference 2016, ASHG 2016 ; Conference date: 18-10-2016 Through 22-10-2016",

url = "http://www.ashg.org/2016meeting/",

}

Cassidy, AJ, Brugnatelli, SV, Ayuso, C, Avila-Fernandez, A, Zeller, D, Lester, DH & The Tayside Centre For Genomic Analysis 2016, 'Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry', American Society of Human Genetics conference 2016, Vancouver, Canada, 18/10/16 - 22/10/16 pp. 1398. <http://www.ashg.org/2016meeting/pdf/ASHG2016-posterabstracts.pdf>

Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry. / Cassidy, A J ; Brugnatelli, S V; Ayuso, C; Avila-Fernandez, A; Zeller, D; Lester, Douglas H.; The Tayside Centre For Genomic Analysis.

2016. 1398 Poster session presented at American Society of Human Genetics conference 2016, Vancouver, Canada.

Research output: Contribution to conference › Poster

TY - CONF

T1 - Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry

AU - Cassidy, A J

AU - Brugnatelli, S V

AU - Ayuso, C

AU - Avila-Fernandez, A

AU - Zeller, D

AU - Lester, Douglas H.

AU - The Tayside Centre For Genomic Analysis

PY - 2016

Y1 - 2016

M3 - Poster

SP - 1398

T2 - American Society of Human Genetics conference 2016

Y2 - 18 October 2016 through 22 October 2016

ER -