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Megalencephaly secondary to a novel germline missense variant p.Asp322Tyr in AKT3 associated with growth hormone deficiency and central hypothyroidism: A case report
Publication with shared reference
10.1002/ajmg.a.63585
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Megalencephaly secondary to a novel germline missense variant p.Asp322Tyr in AKT3 associated with growth hormone deficiency and central hypothyroidism: A case report
Publication with shared reference
10.1002/ajmg.a.63585
Publications with shared reference:
Megalencephaly secondary to a novel germline missense variant p.Asp322Tyr in
AKT3
associated with growth hormone deficiency and central hypothyroidism: A case report
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