Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia
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CHELBAN, Viorica, LYNCH, David S., HOULDEN, Henry H., WOOD, Nick. Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia. In: Journal of Neurology, 2016, vol. 263, pp. 1232-1233. ISSN 0340-5354. DOI: https://doi.org/10.1007/s00415-016-8103-6
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Journal of Neurology
Volumul 263 / 2016 / ISSN 0340-5354 /ISSNe 1432-1459

Triple trouble: a striking new phenotype or competing genes in a family with hereditary spastic paraplegia

DOI:https://doi.org/10.1007/s00415-016-8103-6

Pag. 1232-1233

Chelban Viorica12, Lynch David S.1, Houlden Henry H.1, Wood Nick1
 
1 National Hospital for Neurology and Neurosurgery, Queen Square,
2 ”Nicolae Testemițanu” State University of Medicine and Pharmacy
 
 
Disponibil în IBN: 31 iulie 2022


Cuvinte-cheie
Adenosine Triphosphatases, adult, Diagnosis, differential, family, Humans, Male, Mutation, pedigree, phenotype, Poly(A)-Binding Protein I, skin, Spastic paraplegia, hereditary