Congenital Insensitivity to Pain with Anhidrosis in an Iranian Patient

por Saleh-gohari, Nasrollah, Mohammadi-Anaie, Marzye
Publicado 2013

Haplotype Analysis in Carriers of β-Globin Gene Mutation Facilitates Genetic Counseling in β-Thalassemia: A Cross-Sectional Study in Kerman Province, Iran

por SALEH-GOHARI, Nasrollah, SAEIDI, Kolsoum, ZIAADINI-DASHTKHAKI, Sima
Publicado 2020

The ERCC1/XPF endonuclease is required for efficient single-strand annealing and gene conversion in mammalian cells

por Al-Minawi, Ali Z., Saleh-Gohari, Nasrollah, Helleday, Thomas
Publicado 2008

BRCA1 Gene Mutations in Breast Cancer Patients from Kerman Province, Iran

por Saleh-gohari, Nasrollah, Mohammadi-Anaie, Marzye, Kalantari-Khandani, Behjat
Publicado 2012

A Novel Splice Site Mutation of the ATM Gene Associated with Ataxia Telangiectasia

por SAEIDI, Kolsoum, SALEH GOHARI, Nasrollah, MANSOURI NEJAD, Seyed Ebrahim
Publicado 2018

Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia

por Setoodeh, Aria, Haghighi, Amirreza, Saleh-Gohari, Nasrollah, Ellard, Sian, Haghighi, Alireza
Publicado 2013

Homozygosity Mapping and Whole Exome Sequencing Reveal a Novel Homozygous COL18A1 Mutation Causing Knobloch Syndrome

por Haghighi, Alireza, Tiwari, Amit, Piri, Niloofar, Nürnberg, Gudrun, Saleh-Gohari, Nasrollah, Haghighi, Amirreza, Neidhardt, John, Nürnberg, Peter, Berger, Wolfgang
Publicado 2014

Senior-Loken syndrome secondary to NPHP5/IQCB1 mutation in an Iranian family

por Haghighi, Alireza, Al-Hamed, Mohamed, Al-Hissi, Safa, Hynes, Ann-Marie, Sharifian, Maryam, Roozbeh, Jamshid, Saleh-Gohari, Nasrollah, Sayer, John A.
Publicado 2011

The ERCC1/XPF endonuclease is required for completion of homologous recombination at DNA replication forks stalled by inter-strand cross-links

por Al-Minawi, Ali Z., Lee, Yin-Fai, Håkansson, Daniel, Johansson, Fredrik, Lundin, Cecilia, Saleh-Gohari, Nasrollah, Schultz, Niklas, Jenssen, Dag, Bryant, Helen E., Meuth, Mark, Hinz, John M., Helleday, Thomas
Publicado 2009

Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients

por Haghighi, Alireza, Haack, Tobias B, Atiq, Mehnaz, Mottaghi, Hassan, Haghighi-Kakhki, Hamidreza, Bashir, Rani A, Ahting, Uwe, Feichtinger, René G, Mayr, Johannes A, Rötig, Agnès, Lebre, Anne-Sophie, Klopstock, Thomas, Dworschak, Andrea, Pulido, Nathan, Saeed, Mahmood A, Saleh-Gohari, Nasrollah, Holzerova, Eliska, Chinnery, Patrick F, Taylor, Robert W, Prokisch, Holger
Publicado 2014