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
(Q77500405)
scientific article published on 01 September 1998
scientific article published on 01 September 1998
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description | scientific article published on 01 September 1998 |
External Links
(P356) |
10.1007/S004390050822
|
(P698) |
9799086
|
(P6179) |
1037972753
|