Related Experiment Video
Updated: Jun 29, 2025

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
3.1K
A novel RHD allele caused by c.767 C>T mutation was identified in a Chinese individual
Hongjuan Lyu1, Kun Wang1, Zhihui Feng2
1Obstetrics Department, Qingdao Women and Children's Hospital, Qingdao, P. R. China.
Transfusion
|April 2, 2024
Abstract
No abstract available in PubMed .
More Related Videos
05:51A Strategy to Identify de Novo Mutations in Common Disorders such as Autism and Schizophrenia
Published on: June 15, 2011
25.8K
07:26High-resolution Melting PCR for Complement Receptor 1 Length Polymorphism Genotyping: An Innovative Tool for Alzheimer's Disease Gene Susceptibility Assessment
Published on: July 18, 2017
11.8K