Gathof B.S.,1996

Gathof B.S., Geissler J., Winger A.M., Gresser U. Novel initiation codon mutation Met1THr identified in a patient with partial hypoxanthine phosphoribosyltransferase (HPRT) deficiency. - Hum.Mut., 1996, v. 7, p. 184.

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Табл. HPRT m