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Sporadic case of fatal encephalopathy with neonatal onset associated with a T158M missense mutation in MECP2.
Lynch, S A; Whatley, S D; Ramesh, V; Sinha, S; Ravine, D.
Affiliation
  • Lynch SA; Institute of Human Genetics, International Centre for Life, Central Parkway, Newcastle NE1 3BZ, UK. s.a.lynch@ncl.ac.uk
Arch Dis Child Fetal Neonatal Ed ; 88(3): F250-2, 2003 May.
Article in En | MEDLINE | ID: mdl-12719401
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Brain Diseases / Chromosomal Proteins, Non-Histone / Mutation, Missense / DNA-Binding Proteins Type of study: Risk_factors_studies Limits: Humans / Male / Newborn Language: En Journal: Arch Dis Child Fetal Neonatal Ed Journal subject: PEDIATRIA / PERINATOLOGIA Year: 2003 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Repressor Proteins / Brain Diseases / Chromosomal Proteins, Non-Histone / Mutation, Missense / DNA-Binding Proteins Type of study: Risk_factors_studies Limits: Humans / Male / Newborn Language: En Journal: Arch Dis Child Fetal Neonatal Ed Journal subject: PEDIATRIA / PERINATOLOGIA Year: 2003 Document type: Article Affiliation country: Country of publication: