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array(3) {
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[1936]=>
array(3) {
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[1937]=>
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[1938]=>
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[1939]=>
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[1941]=>
array(3) {
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[1942]=>
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[1943]=>
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[1944]=>
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[1947]=>
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[1948]=>
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[1949]=>
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string(6) "Author"
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[1950]=>
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string(6) "Author"
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string(0) ""
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string(6) "Author"
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string(0) ""
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[1954]=>
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string(6) "Author"
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array(3) {
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string(6) "Author"
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[1956]=>
array(3) {
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string(6) "Author"
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[1957]=>
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string(12) "Slaninová I"
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string(6) "Author"
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string(0) ""
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[1958]=>
array(3) {
["name"]=>
string(8) "Slavov N"
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string(6) "Author"
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string(0) ""
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[1959]=>
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string(9) "Smaili SS"
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string(6) "Author"
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string(0) ""
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string(6) "Author"
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string(0) ""
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[1961]=>
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string(0) ""
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[1962]=>
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string(6) "Author"
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string(6) "Author"
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[1967]=>
array(3) {
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string(10) "Sonawane A"
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string(6) "Author"
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[1968]=>
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[1969]=>
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string(6) "Author"
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[1972]=>
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[1973]=>
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string(6) "Author"
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string(14) "Sotthibundhu A"
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string(0) ""
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string(0) ""
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[1983]=>
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[1984]=>
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string(6) "Author"
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[1985]=>
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[1989]=>
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[2043]=>
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[2044]=>
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[2045]=>
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[2046]=>
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[2047]=>
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[2048]=>
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Publications
The following publications were retrieved from PubMed:
Targeted long-read sequencing identifies missing pathogenic variants in unsolved Werner syndrome cases.
Miller DE, Lee L, Galey M, Kandhaya-Pillai R, Tischkowitz M, Amalnath D, Vithlani A, Yokote K, Kato H, Maezawa Y, Takada-Watanabe A, Takemoto M, Martin GM, Eichler EE, Hisama FM, Oshima J.
J Med Genet. 2022 May 9;
DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome.
Bejaoui Y, Razzaq A, Yousri NA, Oshima J, Megarbane A, Qannan A, Potabattula R, Alam T, Martin GM, Horn HF, Haaf T, Horvath S, El Hajj N.
Aging Cell. 2022 Feb; 2(21)e13555
Werner Syndrome
Oshima J, Martin GM, Hisama FM, Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A.
1993;