Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases | Home page

Orphanet Journal of Rare Diseases

The following new articles have just been published in Orphanet Journal of Rare Diseases RESEARCH Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b) Maryam Eghbali, Maryam Abiri, Saeed Talebi, Zahra Noroozi, Marjan Shakiba, Parastoo Rostami, Hosein Alimadadi, Mehri Najafi, Fatemeh Yazarlou, Ali Rabbani and Mohammad Hossein Modarressi Orphanet Journal of Rare Diseases 2020, 15:35 | Published on: 31 January 2020 Full Text | PDF

Follow BMC on: . For further information or enquiries please use our contact page details. BMC respects your privacy and does not disclose, sell or rent your personal information to any non-affliated third parties with your consent. Privacy policy. BioMed Central Ltd The Campus, 4 Crinan Street, London, N1 9XW, United Kingdom

© 2020 BioMed Central Limited unless otherwise stated. Part of Springer Nature.