Mitochondrial DNA variations and mitochondrial dysfunction in Fanconi anemia

由 Solanki, Avani, Rajendran, Aruna, Mohan, Sheila, Raj, Revathy, Vundinti, Babu Rao
發表在 PLoS One (2020)

Identification of the Fanconi Anemia Complementation Group I Gene, FANCI

由 Dorsman, Josephine C., Levitus, Marieke, Rockx, Davy, Rooimans, Martin A., Oostra, Anneke B., Haitjema, Anneke, Bakker, Sietske T., Steltenpool, Jûrgen, Schuler, Dezsö, Mohan, Sheila, Schindler, Detlev, Arwert, Fré, Pals, Gerard, Mathew, Christopher G., Waisfisz, Quinten, de Winter, Johan P., Joenje, Hans
發表在 Cell Oncol (2007)

A founder variant in the South Asian population leads to a high prevalence of FANCL Fanconi anemia cases in India

由 Donovan, Frank X., Solanki, Avani, Mori, Minako, Chavan, Niranjan, George, Merin, Selvaa, Kumar C, Okuno, Yusuke, Muramastsu, Hideki, Yoshida, Kenichi, Shimamoto, Akira, Takaori-Kondo, Akifumi, Yabe, Hiromasa, Ogawa, Seishi, Kojima, Seiji, Yabe, Miharu, Ramanagoudr-Bhojappa, Ramanagouda, Smogorzewska, Agata, Mohan, Sheila, Rajendran, Aruna, Auerbach, Arleen D, Takata, Minoru, Chandrasekharappa, Settara C., Vundinti, Babu Rao
發表在 Hum Mutat (2019)