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DPM3 gene
Known as:
DOLICHYL-PHOSPHATE MANNOSYLTRANSFERASE 3
, dolichyl-phosphate mannosyltransferase subunit 3
, MGC34275
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National Institutes of Health
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Related topics
Related topics
1 relation
DPM2 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Targeted Next Generation Sequencing Approach Towards Improving Genetic Diagnosis of Limb Girdle Muscular Dystrophy
Katherine Johnson
,
A. Töpf
,
+15 authors
V. Straub
2018
Corpus ID: 209465722
Defects of O-linked glycosylation of alpha-dystroglycan cause a wide spectrum of muscular dystrophies ranging from severe…
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2017
2017
(391) Efficacy and Safety of N1539, Intravenous Meloxicam, in a Phase 3 Study of Subjects with Moderate to Severe Pain following Bunionectomy
R. Pollak
,
I. Gottlieb
,
+6 authors
W. Du
2017
Corpus ID: 78780112
2016
2016
A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophy
P. V. D. Bergh
,
Y. Sznajer
,
+10 authors
V. Straub
Neuromuscular Disorders
2016
Corpus ID: 44323172
2011
2011
Intragenic rearrangements in LARGE and POMGNT1 genes in severe dystroglycanopathies
S. Vuillaumier‐Barrot
,
C. Bouchet-Séraphin
,
+16 authors
N. Seta
Neuromuscular Disorders
2011
Corpus ID: 195684305
2004
2004
Congenital disorder of glycosylation (CDG) type Ie. A new patient
M. Garcı́a-Silva
,
G. Matthijs
,
+8 authors
Paz Briones
Journal of Inherited Metabolic Disease
2004
Corpus ID: 5878710
Summary: CDG Ie is caused by a deficiency of dolichol-phosphate-mannose synthase 1 (DPM1), an enzyme involved in N-glycan…
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