Results
Title

Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin‐deficient congenital muscular dystrophy type 1A.

Authors

Khorrami, Afshin; Goleij, Pouya; Karamad, Vahidreza; Taheri, Elham; Shadman, Behrouz; Emami, Parisa; Jahangirzadeh, Gholamreza; Hajazimian, Saba; Isazadeh, Alireza; Baradaran, Behzad; Heidari, Mansour

Publication

Journal of Clinical Laboratory Analysis, 2021, Vol 35, Issue 11, p1

ISSN

0887-8013

Publication type

Academic Journal

DOI

10.1002/jcla.23930