Original language | English |
---|---|
Pages (from-to) | 344-346 |
Number of pages | 3 |
Journal | Human Mutation |
Volume | 1 |
Issue number | 4 |
DOIs | |
State | Published - 1992 |
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*
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
7
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