403 GGCX Mutations in a Patient With Co-Existent Overlapping PXE/CL Phenotype and Thalassemia Minor

Journal of Investigative Dermatology - United Kingdom
doi 10.1016/j.jid.2019.03.479
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

Extramedullary Hematopoiesis in a Non-Transfused Elderly Patient Diagnosed With Beta Thalassemia Minor

Journal of Hematology and Blood Disorders
2015English

Thalassemia Minor Presenting With Xiphodynia

Journal of Clinical and Analytical Medicine
Medicine
2011English

Acquired Somatic ATRX Mutations in Myelodysplastic Syndrome Associated With Thalassemia (ATMDS) Convey a More Severe Hematologic Phenotype Than Germline ATRX Mutations

Blood
BiochemistryImmunologyCell BiologyHematology
2004English

Overlapping LQT1 and LQT2 Phenotype in a Patient With Long QT Syndrome Associated With Loss-Of-Function Variations in KCNQ1 and KCNH2

Biophysical Journal
Biophysics
2010English

Co-Existent Pulmonary Tuberculosis and Bronchogenic Carcinoma

Postgraduate Medical Journal
Medicine
1956English

Distribution of Β Thalassemia Mutations and Its Correlation With Α Thalassemia in Gujarati Families

International Journal of Human Genetics
Genetics
2003English

Sustained Ventricular Tachycardia in a Patient With Thalassemia Major

Annals of Noninvasive Electrocardiology
MedicineCardiovascular MedicinePhysiologyCardiology
2013English

Β-Thalassemia Minor, Carbohydrate Malabsorption and Histamine Intolerance

Journal of Community Hospital Internal Medicine Perspectives
Internal Medicine
2017English

Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype With ESRD

Journal of the American Society of Nephrology : JASN
MedicineNephrology
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy