Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome.
about
Functional and electrophysiological characterization of four non-truncating mutations responsible for creatine transporter (SLC6A8) deficiency syndrome.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
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2012年学术文章
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2012年学术文章
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2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
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2012年學術文章
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2012年學術文章
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name
Functional and electrophysiolo ...... (SLC6A8) deficiency syndrome.
@en
Functional and electrophysiolo ...... sible for creatine transporter
@nl
type
label
Functional and electrophysiolo ...... (SLC6A8) deficiency syndrome.
@en
Functional and electrophysiolo ...... sible for creatine transporter
@nl
prefLabel
Functional and electrophysiolo ...... (SLC6A8) deficiency syndrome.
@en
Functional and electrophysiolo ...... sible for creatine transporter
@nl
P2093
P2860
P50
P1476
Functional and electrophysiolo ...... (SLC6A8) deficiency syndrome.
@en
P2093
Allel Chabli
Emilie Brulé
Fatna-Léa Makaci
Gabrielle Planelles
Gajja S Salomons
Hervé Toulhoat
Laurence Hubert
Luc Nonnenmacher
Michel Mazzuca
Naziha Bakouh
P2860
P2888
P304
P356
10.1007/S10545-012-9495-9
P577
2012-05-30T00:00:00Z