A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary

Absztrakt
Leírás
Kulcsszavak
Forrás
BMC Medical Genetics. -21 : 61 (2020), p. 1-12. -BMC Med. Genet. - 1471-2350. - 1471-2350