Clinical and biochemical study for the diagnosis, treatment and prenatal diagnosis of tetrahydrobiopterin deficiency due to 6 pyruvoyl tetrahydropterin synthase deficiency / 中华围产医学杂志
Chinese Journal of Perinatal Medicine
;
(12)2003.
Artículo
en Chino
| WPRIM
| ID: wpr-673930
ABSTRACT
G) in PTPS gene were identified in 7 families. The third fetus from two families were not affected by PTPS deficiency.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Tipo de estudio:
Estudio diagnóstico
Idioma:
Chino
Revista:
Chinese Journal of Perinatal Medicine
Año:
2003
Tipo del documento:
Artículo
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