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Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients’ cohort from Qatar. A population specific founder variant
by
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
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Neuromuscular Disorders : Nmd
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Clinical Neurology
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Genomic Modifiers
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Lama2 Founder Mutation In Qatar
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Lama2-Rd
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Life Sciences & Biomedicine
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Mdc1A
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Merosin Deficiency Congenital Muscular Dystrophy
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Neurosciences
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Neurosciences & Neurology
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Osteopenia In Mdc1A
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Science & Technology
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Elsevier
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