(Q77500405)
Statements
Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome (English)
T Tvrdik
S Marcus
S M Hou
S Fält
P Noori
N Podlutskaja
F Hanefeld
P Strømme
1 September 1998