SCOPUS 정보 검색 플랫폼

Volumn 108, Issue 4, 2002, Pages 339-340

Two-loci ADA haplotypes in autistic disorder [2]

(8) Lucarelli, Paola a Saccucci, Patrizia a Bottini, Nunzio b,f De Luca, Danila c Fiumara, Agata d Elia, Maurizio e Porfirio, Maria Cristina f Curatolo, Paolo a,f

a CNR (Italy)

b BURNHAM INSTITUTE (United States)

c Anni Verdi Research Centre for Autism Rome (Italy)

d UNIVERSITY OF CATANIA (Italy)

e OASI RESEARCH INSTITUTE IRCCS (Italy)

f UNIVERSITY OF ROME TOR VERGATA (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE DEAMINASE;

AUTISM; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE STRUCTURE; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; LETTER; MAXIMUM LIKELIHOOD METHOD; PATHOGENESIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADENOSINE DEAMINASE; AUTISTIC DISORDER; GENE FREQUENCY; HAPLOTYPES; HUMANS; ITALY;

EID: 0036532210 PISSN: 01487299 EISSN: None Source Type: Journal
DOI: 10.1002/ajmg.10272 Document Type: Letter

Times cited : (10)

References (8)

1
- 0028906338
- Autism as a strongly genetic disorder: Evidence from a British twin study
- (1995) Psychol Med , vol.25 , pp. 63-77
- Bailey, A.¹ Le Couteur, A.² Gottesman, I.³ Bolton, P.⁴ Simonoff, E.⁵ Yuzda, E.⁶ Rutter, M.⁷

2
- 85047685961
- Autism: Evidence of association with adenosine deaminase genetic polymorphism
- (2001) Neurogenetics , vol.3 , pp. 111-113
- Bottini, N.¹ De Luca, D.² Saccucci, P.³ Fiumara, A.⁴ Elia, M.⁵ Porfirio, M.C.⁶ Lucarelli, P.⁷ Curatolo, P.⁸

3
- 0000826795
- Adenosine deaminase polymorphism in autism
- (1999) J Child Neurol , vol.14 , pp. 323-324
- De Luca, D.¹ Lucarelli, P.² Bottini, N.³ Porfirio, C.⁴ Curatolo, P.⁵

4
- 0030740773
- Cell surface adenosine deaminase: Much more than an ectoenzyme
- (1997) Prog Neurobiol , vol.52 , pp. 283-294
- Franco, R.¹ Casado, V.² Ciruela, F.³ Saura, C.⁴ Mallol, J.⁵ Canela, E.I.⁶ Lluis, C.⁷

5
- 0028292990
- An Asp8Asn substitution results in the adenosine deaminase (ADA) genetic polymorphism (ADA 2 allozyme): Occurrence on different chromosomal backgrounds and apparent intragenic crossover
- (1994) Ann Hum Genet , vol.58 , pp. 1-9
- Hirschhorn, R.¹ Yang, D.R.² Israni, A.³

6
- 0034606332
- Adenosine deaminase alleles and autistic disorder: Case-control and family-based association studies
- (2000) Am J Med Genet , vol.96 , pp. 784-790
- Persico, A.¹ Militerni, R.² Bravaccio, C.³ Schneider, C.⁴ Melmed, R.⁵ Trillo, S.⁶ Montecchi, F.⁷ Palermo, M.T.⁸ Pascucci, T.⁹ Puglisi-Allegra, S.¹⁰ Reichelt, K.L.¹¹ Conciatori, M.¹² Baldi, A.¹³ Keller, F.¹⁴

7
- 0029134874
- Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
- (1995) Am J Hum Genet , vol.57 , pp. 717-726
- Pickles, A.¹ Bolton, P.² Macdonald, H.³ Bailey, A.⁴ Le Couteur, A.⁵ Sim, C.H.⁶ Rutter, M.⁷

8
- 0030764183
- Autism and the immune system
- (1997) J Child Psychol Psychiatry , vol.38 , pp. 337-349
- Van Gent, T.¹ Heijnen, C.J.² Treffers, P.D.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.