The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

Y I YI YANG; Afif HENTATI; Natalie COLE; Generoso GASCON; Ayesha YAGMOUR; Mongi BEN-HAMIDA; Margaret PERICAK-VANCE; Faycal HENTATI; Teepu SIDDIQUE; Han-Xiang DENG; Omar DABBAGH; Toru SASAKI; Makito HIRANO; Wu-Yen HUNG; Karim OUAHCHI; JIANHUA JIANHUA YAN; Anser C AZIM

doi:10.1038/ng1001-160

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The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

Journal article

Peer reviewed

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

Y I YI YANG, Afif HENTATI, Natalie COLE, Generoso GASCON, Ayesha YAGMOUR, Mongi BEN-HAMIDA, Margaret PERICAK-VANCE, Faycal HENTATI, Teepu SIDDIQUE, Han-Xiang DENG, …

Nature genetics, Vol.29(2), pp.160-165

2001

DOI: https://doi.org/10.1038/ng1001-160

PMID: 11586297

Abstract

Fundamental and applied biological sciences. Psychology

Biological and medical sciences

Molecular and cellular biology

Molecular genetics

Genes. Genome

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Collaboration types: Domestic collaboration; International collaboration
Citation topics: 1 Clinical & Life Sciences; 1.52 Neurodegenerative Diseases; 1.52.765 Amyotrophic Lateral Sclerosis
Web Of Science research areas: Genetics & Heredity
ESI research areas: Molecular Biology & Genetics

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Details

Title: The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
Creators: Y I YI YANG - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Afif HENTATI - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Natalie COLE - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Generoso GASCON - Division of Pediatric Neurology, Brown University, Providence, Rhode Island, United States
Ayesha YAGMOUR - King Fahad Military Hospital, Jeddah, Saudi Arabia
Mongi BEN-HAMIDA - Institute of Neurology, Tunis, Tunisia
Margaret PERICAK-VANCE - Medical Genetics, Duke University Medical Center, Durham, North Carolina, United States
Faycal HENTATI - Institute of Neurology, Tunis, Tunisia
Teepu SIDDIQUE - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Han-Xiang DENG - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Omar DABBAGH - King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia
Toru SASAKI - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Makito HIRANO - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Wu-Yen HUNG - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Karim OUAHCHI - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
JIANHUA JIANHUA YAN - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Anser C AZIM - Department of Neurology, Northwestern University Medical School, Chicago, Illinois, United States
Publication Details: Nature genetics, Vol.29(2), pp.160-165
Publisher: Nature Publishing Group; London
Academic Unit: Miller School of Medicine; John P. Hussman Institute for Human Genomics; UMMG Dept of Human Genetics (Dr. John T. Macdonald Foundation)
Language: English
Resource Type: Journal article
PMID: 11586297
Record Identifier: 991031561864302976