Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation.
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Early replacement therapy in a first Japanese case with autosomal recessive guanosine triphosphate cyclohydrolase I deficiency with a novel point mutation.
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2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
Early replacement therapy in a ...... y with a novel point mutation.
@en
Early replacement therapy in a ...... y with a novel point mutation.
@nl
type
label
Early replacement therapy in a ...... y with a novel point mutation.
@en
Early replacement therapy in a ...... y with a novel point mutation.
@nl
prefLabel
Early replacement therapy in a ...... y with a novel point mutation.
@en
Early replacement therapy in a ...... y with a novel point mutation.
@nl
P2093
P1476
Early replacement therapy in a ...... y with a novel point mutation.
@en
P2093
Haruo Shintaku
Hiroki Sato
Naomi Hino-Fukuyo
Osamu Sakamoto
Shigeo Kure
Tojo Nakayama
Tomoko Kobayashi
Wakaba Endo
P304
P356
10.1016/J.BRAINDEV.2013.04.003
P577
2013-05-06T00:00:00Z