| 000 | 01772 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250515004557.0 | ||
| 264 | 0 | _c20060606 | |
| 008 | 200606s 0 0 eng d | ||
| 022 | _a0340-6245 | ||
| 024 | 7 |
_a10.1160/TH05-03-0165 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLiang, Hai Po Helena | |
| 245 | 0 | 0 |
_aA common ancestral glycoprotein (GP) 9 1828A>G (Asn45Ser) gene mutation occurring in European families from Australia and Northern Europe with Bernard-Soulier Syndrome (BSS). _h[electronic resource] |
| 260 |
_bThrombosis and haemostasis _cSep 2005 |
||
| 300 |
_a599-605 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAlleles |
| 650 | 0 | 4 | _aAmino Acid Substitution |
| 650 | 0 | 4 |
_aAustralia _xethnology |
| 650 | 0 | 4 |
_aBernard-Soulier Syndrome _xethnology |
| 650 | 0 | 4 |
_aEurope _xepidemiology |
| 650 | 0 | 4 | _aEvolution, Molecular |
| 650 | 0 | 4 | _aFounder Effect |
| 650 | 0 | 4 | _aHaplotypes |
| 650 | 0 | 4 | _aHeredity |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHomozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aPlatelet Glycoprotein GPIb-IX Complex _xgenetics |
| 650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
| 650 | 0 | 4 | _aSelection, Genetic |
| 650 | 0 | 4 | _aTime Factors |
| 700 | 1 | _aMorel-Kopp, Marie-Christine | |
| 700 | 1 | _aClemetson, Jeannine M | |
| 700 | 1 | _aClemetson, Kenneth J | |
| 700 | 1 | _aKekomaki, Riitta | |
| 700 | 1 | _aKroll, Hartmut | |
| 700 | 1 | _aMichaelides, Katerina | |
| 700 | 1 | _aTuddenham, Edward G D | |
| 700 | 1 | _aVanhoorelbeke, Karen | |
| 700 | 1 | _aWard, Christopher M | |
| 773 | 0 |
_tThrombosis and haemostasis _gvol. 94 _gno. 3 _gp. 599-605 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1160/TH05-03-0165 _zAvailable from publisher's website |
| 999 |
_c15893909 _d15893909 |
||