Homozygous Deletion in MYL9 Expands the Molecular Basis of Megacystis–microcolon–intestinal Hypoperistalsis Syndrome

European Journal of Human Genetics - United Kingdom
doi 10.1038/s41431-017-0055-5
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Megacystis-Microcolon–Intestinal Hypoperistalsis Syndrome

2010English

Cardiac Rhabdomyomata and Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome.

Journal of Medical Genetics
Genetics
1991English

Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome: An Unusual in Utero Presentation

Journal of Ultrasound in Medicine
Nuclear MedicineRadiologyUltrasound TechnologyRadiologicalImagingMedicine
2017English

A Novel Mutation in ACTG2 Gene in Mother With Chronic Intestinal Pseudoobstruction and Fetus With Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Case Reports in Genetics
2017English

Loss of LMOD1 Impairs Smooth Muscle Cytocontractility and Causes Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Humans and Mice

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2017English

Col11a2 Deletion Reveals the Molecular Basis for Tectorial Membrane Mechanical Anisotropy

Biophysical Journal
Biophysics
2009English

The Evaluation of DiGeorge Syndrome Gene Deletion Using Molecular Cytogenetic Techniques

BMC Genomics
BiotechnologyGenetics
2014English

Molecular and Genetic Basis of Inherited Nephrotic Syndrome

International Journal of Nephrology
Nephrology
2011English

Bartter Syndrome in Homozygous Twins

Problemy Endokrinologii
EndocrinologyMetabolismDiabetes
1996English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy