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An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of theRMRPgene associated with chondrodysplasia and severe immunodeficiency

✍ Scribed by N. Vatanavicharn; N. Visitsunthorn; T. Pho-iam; O. Jirapongsananuruk; P. Pacharn; K. Chokephaibulkit; C. Limwongse; P. Wasant


Publisher
Springer-Verlag
Year
2010
Tongue
English
Weight
259 KB
Volume
51
Category
Article
ISSN
1234-1983

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