Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report

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🤖 New article on #MyopiaResearch👁️‍🗨️ indexed in #PubMed https://t.co/2kRLeA0Ceb Related Articles Compound heterozygous POMGNT1 mutations leading to muscular dystrophy-dystroglycanopathy type A3: a case report. BMC Pediatr. 2019 04 08;19(1):98 Authors:

10 Mar 2020

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