Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families

Molecular Vision

Volumn 17, Issue , 2011, Pages 218-224

  Khan, Arif O ^a,b   Shinwari, Jameela ^b   Omar, Aisha ^b   Al Sharif, Latifa ^b   Khalil, Dania S ^b   Alanazi, Mohammed ^c   Al Amri, Abdullah ^c   Al Tassan, Nada ^b  

^a KING KHALED EYE SPECIALIST HOSPITAL   (Saudi Arabia)

^b KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^c KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

BETA TUBULIN; BETA TUBULIN 3; HOMEODOMAIN PROTEIN; KIF21A PROTEIN; KINESIN; PAIRED LIKE HOMEOBOX 2A; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; CONGENITAL FIBROSIS OF THE EXTRACELLULAR MUSCLE TYPE I; CONTROLLED STUDY; EYE DISEASE; FAMILY STUDY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HETEROZYGOSITY; HUMAN; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING;

ADOLESCENT; BLEPHAROPTOSIS; CHILD; CHILD, PRESCHOOL; CONSANGUINITY; DNA PRIMERS; FAMILY HEALTH; FEMALE; GENES, DOMINANT; GENES, RECESSIVE; HETEROZYGOTE; HUMANS; KINESIN; MALE; MUTATION; MUTATION, MISSENSE; OCULOMOTOR MUSCLES; OPHTHALMOPLEGIA; PHENOTYPE; SAUDI ARABIA;

EID: 79551713574     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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