Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.
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Benign Hereditary Chorea: An UpdateNovel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome.Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome.Diiodothyropropionic acid (DITPA) cross-reacts with thyroid function assays on different immunoassay platforms.
P2860
Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.
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2015 nî lūn-bûn
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Redefining the Pediatric Pheno ...... s for Diagnosis and Therapies.
@en
Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8
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type
label
Redefining the Pediatric Pheno ...... s for Diagnosis and Therapies.
@en
Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8
@nl
prefLabel
Redefining the Pediatric Pheno ...... s for Diagnosis and Therapies.
@en
Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8
@nl
P2093
P2860
P356
P1476
Redefining the Pediatric Pheno ...... s for Diagnosis and Therapies.
@en
P2093
Kenton R Holden
Leonardo Bonilha
Maria Gisele Matheus
Rebecca K Lehman
P2860
P304
P356
10.1177/0883073815578524
P577
2015-04-21T00:00:00Z