A 22‐bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family

Sandra Kleiman, Gerard Schwartz, Savio L.C. Woo, Yosef Shiloh

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)344-346
Number of pages3
JournalHuman Mutation
Volume1
Issue number4
DOIs
StatePublished - 1992

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