Mutations in KIF21A and PHOX2A are absent in 16 patients with congenital vertical incomitant strabismus

Ophthalmic Genetics

Volumn 30, Issue 4, 2009, Pages 206-207

  Khan, Arif O ^a,b   Khalil, Dania S ^b   Al Sharif, Latifa J ^b   Al Tassan, Nada A ^b  

^a KING KHALED EYE SPECIALIST HOSPITAL   (Saudi Arabia)

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

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; KINESIN 1; PAIRED MESODERM HOMEOBOX PROTEIN 2A; PROTEIN KIF21A; UNCLASSIFIED DRUG;

BLOOD SAMPLING; BROWN SYNDROME; CONGENITAL STRABISMUS; DUANE RETRACTION SYNDROME; EYE EXAMINATION; GENE IDENTIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; LETTER; MOEBIUS SYNDROME; MYOFIBROSIS; NEUROPATHY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; VERTICAL STRABISMUS;

ADULT; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; HOMEODOMAIN PROTEINS; HUMANS; INFANT; KINESIN; MALE; MUTATION; OPEN READING FRAMES; POLYMERASE CHAIN REACTION; STRABISMUS;

EID: 70350439233     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.3109/13816810903183613     Document Type: Letter

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