Title : Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies.

Pub. Date : 1998 Nov-Dec

PMID : 9856680






2 Functional Relationships(s)
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Protein Name
Organism
1 Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies. Phenylalanine CD1c molecule Homo sapiens
2 CONCLUSION: This report describes the occurrence of Hb Hammersmith [B42(CD1)Phe-->Ser] in African-American twins. Phenylalanine CD1c molecule Homo sapiens