(Q34465484)
Statements
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Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype". (English)
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Statter M
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Ben-Zvi A
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Shina A
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Schein R
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Russell A
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1 August 1976
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173-182
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Identifiers
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