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