Ming-min Gu
280 South Chongqing Road
Shanghai, 200025, China
Shanghai, 200025, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model.
Journal: Acta neuropathologica communications
Published: January 17, 2020
Research progress of myosin heavy chain genes in human genetic diseases.
Journal: Yi chuan = Hereditas
Published: October 27, 2017
The functional mechanisms and clinical application of read-through drugs.
Journal: Yi chuan = Hereditas
Published: October 14, 2016
Advances in genetic studies of Charcot-Marie-Tooth disease type 4 (CMT4)
Journal: Yi chuan = Hereditas
Published: September 10, 2015
Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay.
Journal: Thrombosis research
Published: September 30, 2014
Deletion of Gpr128 results in weight loss and increased intestinal contraction frequency.
Journal: World journal of gastroenterology
Published: June 14, 2013
Nonsense-mediated mRNA decay and human monogenic disease
Journal: Yi chuan = Hereditas
Published: August 25, 2012
A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.
A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.
Journal: American journal of human genetics
Published: May 14, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026