Disease: Neuropathy- hereditary motor and sensory- LOM type
- A novel homozygous NDRG1 mutation in a Chinese patient with Charcot-Marie-Tooth disease 4D
- A novel NDRG1 mutation in a non-Romani patient with CMT4D/HMSN-Lom
- A splice altering variant in NDRG1 gene causes Charcot-Marie-Tooth disease, type 4D
- Aberrant Neuregulin 1/ErbB Signaling in Charcot-Marie-Tooth Type 4D Disease
- Carrier rates of four single-gene disorders in Croatian Bayash Roma
- CMT4D (NDRG1 mutation): genotype-phenotype correlations
- Early clinical and electrophysiologic features of the two most common autosomal recessive forms of Charcot-Marie-Tooth disease in the Roma (Gypsies)
- Exonic duplication CNV of NDRG1 associated with autosomal-recessive HMSN-Lom/CMT4D
- Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia
- Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depth
- Hereditary motor and sensory neuropathy Lom type in a Serbian family
- Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family
- Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
- Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studies
- Hereditary motor and sensory neuropathy, LOM type (HMSNL)
- HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 8
- HMSNL in a 13-year-old Bulgarian girl
- HSMNR belongs to the most frequent types of hereditary neuropathy in the Czech Republic and is twice more frequent than HMSNL
- Identification and functional characterization of two missense mutations in NDRG1 associated with Charcot-Marie-Tooth disease type 4D
- Impaired differentiation of macrophage lineage cells attenuates bone remodeling and inflammatory angiogenesis in Ndrg1 deficient mice
- Molecular functions of the iron-regulated metastasis suppressor, NDRG1, and its potential as a molecular target for cancer therapy
- NDRG1 functions in LDL receptor trafficking by regulating endosomal recycling and degradation
- Ndrg1 in development and maintenance of the myelin sheath
- Ndrg1-deficient mice exhibit a progressive demyelinating disorder of peripheral nerves
- Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary
- The electrophysiological profile of hereditary motor and sensory neuropathy-Lom
- The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies
- The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4