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Establishing the UK DNA Bank for motor neuron disease (MND).Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears.Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.Evidence of Inbreeding in Hodgkin Lymphoma.Inbreeding and homozygosity in breast cancer survival.Identification of a de novo DYNC1H1 mutation via WES according to published guidelines.Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population.
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 24 April 2013
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Homozygosity analysis in amyotrophic lateral sclerosis.
@en
Homozygosity analysis in amyotrophic lateral sclerosis.
@nl
type
label
Homozygosity analysis in amyotrophic lateral sclerosis.
@en
Homozygosity analysis in amyotrophic lateral sclerosis.
@nl
prefLabel
Homozygosity analysis in amyotrophic lateral sclerosis.
@en
Homozygosity analysis in amyotrophic lateral sclerosis.
@nl
P2093
P2860
P50
P356
P1476
Homozygosity analysis in amyotrophic lateral sclerosis.
@en
P2093
Bryan J Traynor
Chris E Shaw
Hannu Laaksovirta
Liisa Myllykangas
Michael A Nalls
Nicole Gurunlian
Pentti J Tienari
Richard W Orrell
Terhi Peuralinna
P2860
P2888
P304
P356
10.1038/EJHG.2013.59
P50
P577
2013-04-24T00:00:00Z