A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy.

Saved in:

Bibliographic Details
Title:	A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy.
Authors:	Chausova PA; Research Centre for Medical Genetics named after academician N.P. Bochkov, Ministry of Education and Science of the Russian Federation, Moscow, Russia., Ryzhkova OP; Research Centre for Medical Genetics named after academician N.P. Bochkov, Ministry of Education and Science of the Russian Federation, Moscow, Russia., Rudenskaya GE; Research Centre for Medical Genetics named after academician N.P. Bochkov, Ministry of Education and Science of the Russian Federation, Moscow, Russia., Chernykh VB; Research Centre for Medical Genetics named after academician N.P. Bochkov, Ministry of Education and Science of the Russian Federation, Moscow, Russia., Shchagina OA; Research Centre for Medical Genetics named after academician N.P. Bochkov, Ministry of Education and Science of the Russian Federation, Moscow, Russia., Polyakov AV; Research Centre for Medical Genetics named after academician N.P. Bochkov, Ministry of Education and Science of the Russian Federation, Moscow, Russia.
Source:	Frontiers in genetics [Front Genet] 2021 Oct 29; Vol. 12, pp. 686800. Date of Electronic Publication: 2021 Oct 29 (Print Publication: 2021).
Publication Type:	Case Reports; Journal Article
Journal Info:	Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1664-8021
DOI:	10.3389/fgene.2021.686800