A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism. [electronic resource]
Producer: 20170315Description: 3460234 p. digitalISSN:- 2314-6141
- Amino Acid Motifs
- Chromosomes -- ultrastructure
- Cognition Disorders -- genetics
- Computational Biology
- Disease Progression
- Exons
- Homozygote
- Humans
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 -- genetics
- Levodopa -- therapeutic use
- Male
- Middle Aged
- Morocco
- Mutation
- Mutation, Missense
- Oligonucleotide Array Sequence Analysis
- Parkinson Disease -- drug therapy
- Pedigree
- Phenotype
- Protein Domains
- Protein Kinases -- genetics
- Sequence Analysis, DNA
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Publication Type: Case Reports; Journal Article
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