A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.

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Bibliographic Details
Title: A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy.
Authors: Nejati, Parham1,2 (AUTHOR), Falsafi, Nafiseh3 (AUTHOR), Alimoradi, Elham4 (AUTHOR), Khosravi, Teymoor5,6 (AUTHOR), Kamari, Mohana1 (AUTHOR), Oladnabi, Morteza6,7 (AUTHOR) oladnabidozin@yahoo.com, Alibakhshi, Reza1,4 (AUTHOR) ralibakhshi@kums.ac.ir
Source: BMC Medical Genomics. 11/4/2025, Vol. 18 Issue 1, p1-9. 9p.
Database: Academic Search Ultimate
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