Study of Mendelian forms of Crohn's disease in Saudi Arabia reveals novel risk loci and alleles

Gut

Volumn 63, Issue 11, 2014, Pages 1831-1832

  Patel, Nisha ^a   El Mouzan, Mohammad I ^b   Al Mayouf, Sulaiman M ^a   Adly, Nouran ^a   Mohamed, Jawahir Y ^a   Al Mofarreh, Mohammad A ^c   Ibrahim, Niema ^a   Xiong, Yong ^d   Zhao, Qi ^d   Al Saleem, Khalid A ^a   Alkuraya, Fowzan S ^a,e  

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

^b KING SAUD UNIVERSITY   (Saudi Arabia)

^c Al Mofarreh Polyclinics ^*  (Saudi Arabia)

^d YALE UNIVERSITY   (United States)

^e ALFAISAL UNIVERSITY   (Saudi Arabia)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID;

ALLELE; ARTHROPATHY; AUTOSOMAL RECESSIVE INHERITANCE; AUTOZYGOSITY MAPPING; CLINICAL ARTICLE; CROHN DISEASE; EXOME; GAL3ST2 GENE; GAL3ST4 GENE; GENE; GENE LOCUS; GENE MAPPING; GENE SEQUENCE; GENETIC ASSOCIATION; HAPLOTYPE; HUMAN; INFLAMMATORY BOWEL DISEASE; LACC1 GENE; LETTER; MENDELIAN CROHN DISEASE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; ONSET AGE; SAUDI ARABIA; SINGLE NUCLEOTIDE POLYMORPHISM; GENETIC PREDISPOSITION; GENETICS;

GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFLAMMATORY BOWEL DISEASES;

EID: 84907696889     PISSN: 00175749     EISSN: 14683288     Source Type: Journal    
DOI: 10.1136/gutjnl-2014-307859     Document Type: Letter

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