NOTCH3 mutations and clinical features in 33 mainland Chinese families with CADASIL

Journal of Neurology, Neurosurgery and Psychiatry

Volumn 82, Issue 5, 2011, Pages 524-533

  Wang, Zhaoxia ^a   Yuan, Yun ^a   Zhang, Wei ^a   Lv, He ^a   Hong, Daojun ^a   Chen, Bin ^a   Liu, Yang ^a   Luan, Xinghua ^a   Xie, Sheng ^a   Wu, Shiwen ^b  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

^b General Hospital of the Armed Police Forces   (China)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH3 RECEPTOR; SERINE; THREONINE; NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN;

ADULT; AGED; ALOPECIA; AMINO ACID SUBSTITUTION; ANXIETY; ARTICLE; BONE BIOPSY; BRAIN DISEASE; BRAIN INFARCTION; BRAIN STEM INJURY; CADASIL; CHINA; CLINICAL ARTICLE; CLINICAL FEATURE; CODON; COGNITIVE DEFECT; CONTROLLED STUDY; DEPRESSION; EXON; FEMALE; GENE MUTATION; GENE SEQUENCE; HEARING IMPAIRMENT; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; IRRITABILITY; LEUKOARAIOSIS; MALE; MANIA; MIGRAINE WITH AURA; MUTATIONAL ANALYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SKIN BIOPSY; STROKE; SURAL NERVE; SYMPTOMATOLOGY; TINNITUS; TRANSIENT ISCHEMIC ATTACK; BRAIN; GENE DELETION; GENETIC ASSOCIATION; GENETICS; MISSENSE MUTATION; MUTATION; PATHOLOGY; SINGLE NUCLEOTIDE POLYMORPHISM; CHINESE; FAMILIAL DISEASE; GENE FREQUENCY; GENE IDENTIFICATION; LACUNAR STROKE; MUTATOR GENE; NERVE BIOPSY; NOTCH3 GENE; SEQUENCE ANALYSIS; SMOOTH MUSCLE FIBER; WHITE MATTER LESION;

BRAIN; CADASIL; CHINA; GENETIC ASSOCIATION STUDIES; HUMANS; MAGNETIC RESONANCE IMAGING; MUTATION; MUTATION, MISSENSE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, NOTCH; SEQUENCE DELETION;

EID: 79953887891     PISSN: 00223050     EISSN: 1468330X     Source Type: Journal    
DOI: 10.1136/jnnp.2010.209247     Document Type: Article

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