Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

Evidence of Two Novel LAMA2 Variants in a Patient with Muscular Dystrophy: Facing the Challenges of a Certain Diagnosis

Stefanie Meyer,Silke Kaulfuss,Sabrina Zechel,Karsten Kummer,Ali Seif Amir Hosseini,Marielle Sophie Ernst,Jens Schmidt,Silke Pauli,Jana Zschuentzsch

FRONTIERS IN NEUROLOGY（2022）

Cited 1|Views33
Key words
muscular dystrophy,LGMDR23,hereditary myopathy,merosin,next generation sequencing
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined