Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.

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Bibliographic Details
Title: Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.
Authors: Ghanei, Mahmoud1,2, Sadat Fatemi, Seyedeh Helia1,2, Soudyab, Mohammad1, Esfehani, Reza Jafarzadeh2 drrezajafarzadeh@yahoo.com
Source: Neurology Asia. 2022, Vol. 27 Issue 4, p955-962. 8p.
Database: Academic Search Ultimate
Description
ISSN:18236138
DOI:10.54029/2022jdc