Disease: Leber congenital amaurosis

Human Genetics

Volumn 127, Issue 4, 2010, Pages 487-

  Vallespin, E ^a   Avila Fernandez, A ^a   Almoguera, B ^a   Velez Monsalve, C ^a   Cantalapiedra, D ^a   Garcia Hoyos, M ^a   Riveiro Alvarez, R ^a   Aguirre Lamban, J ^a   Bustamante Aragones, A ^a   Trujillo Tiebas, M J ^a   Ayuso, C ^a  

^a Hospital UniversitarioFundación Jiménez Díaz   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

LCA5 PROTEIN; NUCLEOTIDE; PROLINE; PROTEIN; SERINE; UNCLASSIFIED DRUG; EYE PROTEIN; LEBERCILIN PROTEIN, HUMAN; MICROTUBULE ASSOCIATED PROTEIN;

AMINO ACID SUBSTITUTION; BASE PAIRING; CODON; LEBER CONGENITAL AMAUROSIS; MISSENSE MUTATION; NONSENSE MUTATION; NOTE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; ARTICLE; GENETICS; HUMAN;

AMINO ACID SUBSTITUTION; BASE SEQUENCE; CODON; EYE PROTEINS; HUMANS; LEBER CONGENITAL AMAUROSIS; MICROTUBULE-ASSOCIATED PROTEINS; MUTATION, MISSENSE;

EID: 84863679090     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: None     Document Type: Note

References (0)