scholarly article | Q13442814 |
P356 | DOI | 10.1086/424822 |
P8608 | Fatcat ID | release_3gfj22k2bnhi7kk33ewn6ddniq |
P932 | PMC publication ID | 1182067 |
P5875 | ResearchGate publication ID | 25007493 |
P2093 | author name string | Salomons GS | |
Ropers H | |||
P2860 | cites work | High prevalence of SLC6A8 deficiency in X-linked mental retardation | Q24533559 |
Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation | Q28186625 | ||
Nonsyndromic X-linked mental retardation: where are the missing mutations? | Q34205119 | ||
Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation. | Q42930411 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 731-732 | |
P577 | publication date | 2004-10-01 | |
P1433 | published in | American Journal of Human Genetics | Q4744249 |
P1476 | title | Reply to Mandel | |
P478 | volume | 75 |