Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290

Saeed Reza Ghaffari, M. Rafati, G. Ghaffari, M. Morra, Mustafa Tekin

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)387-390
Number of pages4
JournalClinical Genetics
Volume86
Issue number4
DOIs
StatePublished - Jan 1 2014

Fingerprint

Neoplasm Proteins
Neoplasm Antigens
Preschool Children
Iran
Intellectual Disability
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics

Cite this

Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290. / Ghaffari, Saeed Reza; Rafati, M.; Ghaffari, G.; Morra, M.; Tekin, Mustafa.

In: Clinical Genetics, Vol. 86, No. 4, 01.01.2014, p. 387-390.

Research output: Contribution to journalArticle

Ghaffari, Saeed Reza ; Rafati, M. ; Ghaffari, G. ; Morra, M. ; Tekin, Mustafa. / Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290. In: Clinical Genetics. 2014 ; Vol. 86, No. 4. pp. 387-390.
@article{623a9fd4688c4344b61dacbd08830a06,
title = "Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290",
author = "Ghaffari, {Saeed Reza} and M. Rafati and G. Ghaffari and M. Morra and Mustafa Tekin",
year = "2014",
month = "1",
day = "1",
doi = "10.1111/cge.12296",
language = "English",
volume = "86",
pages = "387--390",
journal = "Clinical Genetics",
issn = "0009-9163",
publisher = "Wiley-Blackwell",
number = "4",

}

TY - JOUR

T1 - Familial intellectual disability in an Iranian family with a novel truncating mutation in CEP290

AU - Ghaffari, Saeed Reza

AU - Rafati, M.

AU - Ghaffari, G.

AU - Morra, M.

AU - Tekin, Mustafa

PY - 2014/1/1

Y1 - 2014/1/1

UR - http://www.scopus.com/inward/record.url?scp=84908226957&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=84908226957&partnerID=8YFLogxK

U2 - 10.1111/cge.12296

DO - 10.1111/cge.12296

M3 - Article

C2 - 24175892

AN - SCOPUS:84908226957

VL - 86

SP - 387

EP - 390

JO - Clinical Genetics

JF - Clinical Genetics

SN - 0009-9163

IS - 4

ER -