Charcot-Marie-Tooth Disease Type 1a (CMT1a): Evidence for Trisomy of the Region P11.2 of Chromosome 17 in South Wales Families.

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.29.1.12
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

Erratum To: Respiratory Dysfunction in Charcot–Marie–Tooth Disease Type 1A

Journal of Neurology
Neurology
2015English

High-Dosage Ascorbic Acid Treatment in Charcot-Marie-Tooth Disease Type 1A

JAMA Neurology
Neurology
2013English

Hidden Hearing Loss in Patients With Charcot-Marie-Tooth Disease Type 1A

Scientific Reports
Multidisciplinary
2018English

Gait Pattern Classification in Children With Charcot–Marie–Tooth Disease Type 1A

Gait and Posture
Sports ScienceOrthopedicsSports MedicineRehabilitationBiophysics
2012English

Charcot-Marie-Tooth Disease Type 2R

2020English

Charcot-Marie-Tooth Disease Type 2B5

2020English

Charcot-Marie-Tooth Disease Type 4G

2020English

Antisense Oligonucleotides Offer Hope to Patients With Charcot-Marie-Tooth Disease Type 1A

Journal of Clinical Investigation
Medicine
2017English

Charcot–Marie–Tooth Disease

2012English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy