N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy

N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom

Published:2000-07 Issue:1 Volume:67 Page:47-58
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Kalaydjieva Luba,Gresham David,Gooding Rebecca,Heather Lisa,Baas Frank,de Jonge Rosalein,Blechschmidt Karin,Angelicheva Dora,Chandler David,Worsley Penelope,Rosenthal Andre,King Rosalind H.M.,Thomas P.K.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference54 articles.

1. Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group;Antonarakis;Hum Mutat,1998

2. Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development;Baechner;J Neurosci Res,1995

3. HMSNL in a 13-year-old Bulgarian girl;Baethmann;Neuromuscul Disord,1998

4. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q;Ben Othmane;Hum Mol Genet,1993

5. A rapid alkaline extraction procedure for screening recombinant plasmid DNA;Birnboim;Nucleic Acids Res,1979

Cited by 320 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. Identification and Characterization of Novel Founder Mutations in NDRG1: Refining the Genetic Landscape of Charcot–Marie–Tooth Disease Type 4D in Bulgaria;International Journal of Molecular Sciences;2024-08-21

2. Transcriptome- and proteome-wide effects of a circular RNA encompassing four early exons of the spinal muscular atrophy genes;2024-02-28

3. Irrespective of Plaque Activity, Multiple Sclerosis Brain Periplaques Exhibit Alterations of Myelin Genes and a TGF-Beta Signature;International Journal of Molecular Sciences;2022-11-30

4. NDRG1 is induced by antigen-receptor signaling but dispensable for B and T cell self-tolerance;Communications Biology;2022-11-10

5. Aberrant Neuregulin 1/ErbB Signaling in Charcot-Marie-Tooth Type 4D Disease;Molecular and Cellular Biology;2022-07-01