rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Neurological presentation of a congenital disorder of glycosylation CDG-Ia: implications for diagnosis and genetic counseling.
11343337
2001
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Mitotic Intragenic Recombination: A Mechanism of Survival for Several Congenital Disorders of Glycosylation.
26805780
2016
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
The Effects of PMM2-CDG-Causing Mutations on the Folding, Activity, and Stability of the PMM2 Protein.
26014514
2015
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Three families with mild PMM2-CDG and normal cognitive development.
28425223
2017
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Carbohydrate-deficient glycoprotein syndrome type 1A: expression and characterisation of wild type and mutant PMM2 in E. coli.
10602363
1999
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
A new insight into PMM2 mutations in the French population.
15844218
2005
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome).
9140401
1997
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Phosphomannomutase deficiency: the molecular basis of the classical Jaeken syndrome (CDGS type Ia).
10527672
1999
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Lack of Hardy-Weinberg equilibrium for the most prevalent PMM2 mutation in CDG-Ia (congenital disorders of glycosylation type Ia).
10854097
2000
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Heterodimerization of Two Pathological Mutants Enhances the Activity of Human Phosphomannomutase2.
26488408
2015
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2.
28373276
2017
rs28936415
×
Entrez Id:
5373
Gene Symbol:
PMM2
PMM2
Movement Disorders
A
0.700
CausalMutation
CLINVAR
Biochemical phenotype of a common disease-causing mutation and a possible therapeutic approach for the phosphomannomutase 2-associated disorder of glycosylation.
24498599
2013