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An atypical presentation of severe congenital contractures and lack of cerebellar involvement in a patient with a novel LAMA1 mutation
by
Ammari, Ameur
,
Alhashem, Amal
,
Abdelraouf, Hanen
,
Alzahrani, Fatma
,
Alkuraya, Fowzan
,
Tabarki, Brahim
Published in
Journal of Biochemical and Clinical Genetics
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Journal Of Biochemical And Clinical Genetics
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Arthrogryposis
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Case Report
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Cerebellum
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Lama1 Gene
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Doaj Directory Of Open Access Journals
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