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Wolcott–Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature

✍ Scribed by M Nuri Ozbek; Valérie Senée; Sehnaz Aydemir; L Damla Kotan; Neslihan O Mungan; Bilgin Yuksel; Cécile Julier; A Kemal Topaloglu

No coin nor oath required. For personal study only.

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