Ben El Haj, Rafiqua <br/><br/>
A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.  [electronic resource] 

 -  BioMed research international  2016 
 - 3460234 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>2314-6141 
<br/><br/><label>Standard No.: </label>10.1155/2016/3460234  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Motifs<br/>Chromosomes--ultrastructure<br/>Cognition Disorders--genetics<br/>Computational Biology<br/>Disease Progression<br/>Exons<br/>Homozygote<br/>Humans<br/>Leucine-Rich Repeat Serine-Threonine Protein Kinase-2--genetics<br/>Levodopa--therapeutic use<br/>Male<br/>Middle Aged<br/>Morocco<br/>Mutation<br/>Mutation, Missense<br/>Oligonucleotide Array Sequence Analysis<br/>Parkinson Disease--drug therapy<br/>Pedigree<br/>Phenotype<br/>Protein Domains<br/>Protein Kinases--genetics<br/>Sequence Analysis, DNA