Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome

Kobe Journal of Medical Sciences

Volumn 53, Issue 4, 2007, Pages 157-162

  Sasongko, Teguh Haryo ^a   Hamim, Ahmad ^a   Gunadi, ^a   Myeong, Jin Lee ^a   Koterazawa, Keiko ^b   Nishio, Hisahide ^a  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b Himeji City Center for the Handicapped   (Japan)

Author keywords

Mowat Wilson syndrome; Nonsense mutation; SIP1; ZFHX1B

Indexed keywords

ARTICLE; CASE REPORT; CHILD; CLINICAL FEATURE; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; HIRSCHSPRUNG DISEASE; HUMAN; MENTAL DEFICIENCY; MOLECULAR GENETICS; MOWAT WILSON SYNDROME; NONSENSE MUTATION; POLYMERASE CHAIN REACTION; ZINC FINGER HOMEOBOX 1B GENE;

EID: 84946396869     PISSN: 00232513     EISSN: 18830498     Source Type: Journal    
DOI: None     Document Type: Article

References (12)

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