A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
about
Active transport of the ubiquitin ligase MID1 along the microtubules is regulated by protein phosphatase 2AThe Challenge of Prenatal Diagnostic Work-Up of Maternally Inherited X-Linked Opitz G/BBB: Case Report and Literature Review.Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndrome.X-linked Opitz G/BBB syndrome: identification of a novel mutation and prenatal diagnosis in a Korean family.Multifaceted roles of TRIM38 in innate immune and inflammatory responses.Dental treatment of a patient with Opitz G/BBB syndrome.Two Novel Pathogenic MID1 Variants and Genotype-Phenotype Correlation Reanalysis in X-Linked Opitz G/BBB Syndrome.A MID1 gene mutation in a patient with Opitz G/BBB syndrome that altered the 3D structure of SPRY domain.
P2860
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P2860
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
description
2006 nî lūn-bûn
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2006年の論文
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2006年論文
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2006年論文
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2006年論文
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2006年論文
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name
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@ast
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@en
type
label
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@ast
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@en
prefLabel
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@ast
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@en
P2093
P1476
A structure-function study of MID1 mutations associated with a mild Opitz phenotype.
@en
P2093
Germana Meroni
Hassan Al-Ali Merheby
Laila Mnayer
Louis J Elsas
Sawsan Khuri
P304
P356
10.1016/J.YMGME.2005.10.014
P577
2006-03-01T00:00:00Z