Gene symbol: AIPL1. Disease: LCA4.

Human genetics

Volumn 116, Issue 6, 2005, Pages 542-

  Khaliq, S ^a   Abid, Aiysha ^a   Hameed, Abdul ^a   Anwar, Khalid ^a   Mohyuddin, Aisha ^a   Ismail, Muhammad ^a   Mehdi, S Qasim ^a  

^a Dr A Q Khan Research Laboratories   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

AIPL1 PROTEIN, HUMAN; CARRIER PROTEIN;

AMINO ACID SUBSTITUTION; ARTICLE; GENETICS; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; MISSENSE MUTATION;

AMINO ACID SUBSTITUTION; CARRIER PROTEINS; HUMANS; MUTATION, MISSENSE; OPTIC ATROPHY, HEREDITARY, LEBER;

EID: 21444440113     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)