Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation.
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Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation updateGenetics of Parkinson diseaseParkin-deficient mice are not more sensitive to 6-hydroxydopamine or methamphetamine neurotoxicityA Peruvian family with a novel PARK2 mutation: Clinical and pathological characteristicsTwenty years since the discovery of the parkin gene.Tensile properties in collagen-rich tissues of Quarter Horses with hereditary equine regional dermal asthenia (HERDA).Parkin gene alterations in hepatocellular carcinoma.Comparative genomic hybridization solves a 14-year-old PARKIN mystery.
P2860
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P2860
Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation.
description
2003 nî lūn-bûn
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2003年の論文
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年学术文章
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2003年學術文章
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name
Marked variation in clinical p ...... heterozygous parkin mutation.
@en
Marked variation in clinical p ...... heterozygous parkin mutation.
@nl
type
label
Marked variation in clinical p ...... heterozygous parkin mutation.
@en
Marked variation in clinical p ...... heterozygous parkin mutation.
@nl
prefLabel
Marked variation in clinical p ...... heterozygous parkin mutation.
@en
Marked variation in clinical p ...... heterozygous parkin mutation.
@nl
P2093
P50
P356
P1433
P1476
Marked variation in clinical p ...... heterozygous parkin mutation.
@en
P2093
J William Langston
Louis C Tan
P304
P356
10.1002/MDS.10432
P407
P577
2003-07-01T00:00:00Z