Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant
Abdel Aleem, Alice, Elsaid, Mahmoud F., Chalhoub, Nader, Chakroun, Almahdi, Mohamed, Khalid A.S., AlShami, Rana, Kuzu, Omer, Mohamed, Reem B., Ibrahim, Khalid, AlMudheki, Noora, Osman, Omar, Ross, M. Elizabeth, ELalamy, Osama
Published in Neuromuscular disorders : NMD (01.06.2020)
Published in Neuromuscular disorders : NMD (01.06.2020)
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