Title : Identification and rapid detection of three Tay-Sachs mutations in the Moroccan Jewish population.

Pub. Date : 1992 Aug

PMID : 1322637






1 Functional Relationships(s)
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1 Elsewhere we reported an in-frame deletion of one of the two adjacent phenylalanine codons at position 304 or 305 (delta F304/305) in one HEXA allele of a Moroccan Jewish TSD patient and in three obligate carriers from six unrelated Moroccan Jewish families. Phenylalanine hexosaminidase subunit alpha Homo sapiens