A polymerase chain reaction-based genotyping assay for detecting a novel Sandhoff disease-causing mutation.
about
Incidence and carrier frequency of Sandhoff disease in Saskatchewan determined using a novel substrate with detection by tandem mass spectrometry and molecular genetic analysis.Late adult-onset pure spinal muscular atrophy due to a compound HEXB macro-deletion.Advances in Human Biology: Combining Genetics and Molecular Biophysics to Pave the Way for Personalized Diagnostics and Medicine
P2860
A polymerase chain reaction-based genotyping assay for detecting a novel Sandhoff disease-causing mutation.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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name
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@en
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@nl
type
label
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@en
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@nl
prefLabel
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@en
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@nl
P2093
P356
P1476
A polymerase chain reaction-ba ...... hoff disease-causing mutation.
@en
P2093
Braden B Fitterer
Denis C Lehotay
Nick A Antonishyn
P304
P356
10.1089/GTMB.2011.0215
P577
2011-12-22T00:00:00Z