SCOPUS 정보 검색 플랫폼

The Lancet Neurology

Volumn 15, Issue 6, 2016, Pages 538-540

Chromosomal deletion at 22q11.2 and Parkinson's disease

(1) Tan, Eng King a

a SINGAPORE GENERAL HOSPITAL (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME 22; CHROMOSOME DELETION 22Q11; COPY NUMBER VARIATION; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SCREENING; HUMAN; MISSENSE MUTATION; NOTE; ONSET AGE; PARKINSON DISEASE; PHENOTYPE; PRIORITY JOURNAL; DIGEORGE SYNDROME;

DIGEORGE SYNDROME; HUMANS; PARKINSON DISEASE;

EID: 84962829123 PISSN: 14744422 EISSN: 14744465 Source Type: Journal
DOI: 10.1016/S1474-4422(16)00115-0 Document Type: Note

Times cited : (3)

References (7)

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2
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- The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome
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3
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- Chromosome 22q11.2 deletion may contain a locus for recessive early-onset Parkinson's disease
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- (2014) Parkinsonism Relat Disord , vol.20 , pp. 945-946
- Ogaki, K.¹ Ross, O.A.²

4
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- Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: identification of a novel genetic form of Parkinson disease and its clinical implications
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5
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- Deletions at 22q11.2 in idiopathic Parkinson's disease: a retrospective combined analysis of genome-wide association data
- published online March 23.
- Mok KY, Sheerin U, Simón-Sánchez J, et al. Deletions at 22q11.2 in idiopathic Parkinson's disease: a retrospective combined analysis of genome-wide association data. Lancet Neurol 2016, published online March 23. http://dx.doi.org/10.1016/S1474-4422(16)00071-5.
- (2016) Lancet Neurol
- Mok, K.Y.¹ Sheerin, U.² Simón-Sánchez, J.³

6
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7
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- Rare and common LRRK2 exonic variants in Parkinson's disease
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- Tan, E.K.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.