Localization of the Gene for Distal Hereditary Motor Neuronopathy VII (dHMN-VII) to Chromosome 2q14-Reference-Cited by-同舟云学术

Localization of the Gene for Distal Hereditary Motor Neuronopathy VII (dHMN-VII) to Chromosome 2q14

Published:2001-05 Issue:5 Volume:68 Page:1270-1276
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

McEntagart Meriel,Norton Nadine,Williams Hywel,Teare M. Dawn,Dunstan Melanie,Baker Philip,Houlden Henry,Reilly Mary,Wood Nick,Harper Peter S.,Futreal P. Andrew,Williams Nigel,Rahman Nazneen

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference24 articles.

1. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?;Boltshauser;J Med Genet,1989

2. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy;Brais;Nat Genet,1998

3. Mapping of a distal form of spinal muscular atrophy with upper limb predominance to chromosome 7p;Christodoulou;Hum Mol Genet,1995

4. A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12;Christodoulou;Ann Neurol,2000

5. Expression patterns of the homeo box-containing genes En-1 and En-2 and the proto-oncogene int-1 diverge during mouse development;Davis;Genes Dev,1988

Cited by 59 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary Motor Neuropathy;Reference Module in Neuroscience and Biobehavioral Psychology;2024

2. Functional and Biochemical Consequences of Disease Variants in Neurotransmitter Transporters: A Special Emphasis on Folding and Trafficking Deficits;Pharmacology & Therapeutics;2021-06

3. Research in Speech Science and Voice Disorders: The Promise of Modern Genetic Approaches in Improving Clinical Diagnosis and Treatment;Perspectives of the ASHA Special Interest Groups;2020-11-23

4. Choline transporter mutations in severe congenital myasthenic syndrome disrupt transporter localization;Brain;2017-10-27

5. Vocal cord paralysis in Charcot–Marie–Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature;Neuromuscular Disorders;2017-05