SLC12A Ion Transporter Mutations in Sporadic and Familial Human Congenital Hydrocephalus

Molecular genetics & genomic medicine - United States
doi 10.1002/mgg3.892
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Lipoprotein Particle Profiles Mark Familial and Sporadic Human Longevity

PLoS Medicine
BiochemistryBiotechnologyMolecular BiologyCell BiologyMedicine
2006English

LINE-1 Hypomethylation in Familial and Sporadic Cancer

Journal of Molecular Medicine
Molecular MedicineDrug DiscoveryGenetics
2012English

Sporadic and Familial Cases of Aquagenic Keratoderma

Journal of Dermatological Case Reports
Dermatology
2016English

LKB1 Somatic Mutations in Sporadic Tumors

American Journal of Pathology
Forensic MedicinePathology
1999English

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus

Neuron
Neuroscience
2018English

Hydrocephalus and Endocarditis in a Congenital Syphilitic Mental Defective

Sexually Transmitted Infections
DermatologyInfectious Diseases
1933English

Differences in Survival for Patients With Familial and Sporadic Cancer

International Journal of Cancer
Cancer ResearchOncology
2016English

Congenital Familial Nodal Rhythm

Circulation
Cardiovascular MedicinePhysiologyCardiology
1960English

2.Congenital Hydrocephalus : Standard Treatment and Its Result

Japanese Journal of Neurosurgery
SurgeryNeurology
2003English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy