<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Thodi, G.</style></author><author><style face="normal" font="default" size="100%">Schulpis, K.H.</style></author><author><style face="normal" font="default" size="100%">Hatzidaki, M.</style></author><author><style face="normal" font="default" size="100%">Molou, E.</style></author><author><style face="normal" font="default" size="100%">Triantafylli, O.</style></author><author><style face="normal" font="default" size="100%">Dotsikas, Y.</style></author><author><style face="normal" font="default" size="100%">Loukas, Y.L.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Partial biotinidase deficiency: Identification of a single novel mutation (p.H314R) in a Greek newborn</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Pediatric Endocrinology and Metabolism</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.scopus.com/inward/record.uri?eid=2-s2.0-84960954904&amp;partnerID=40&amp;md5=7ba60e2e4ecb5b265db7829fa11b507b</style></url></web-urls></urls><number><style face="normal" font="default" size="100%">3</style></number><volume><style face="normal" font="default" size="100%">29</style></volume><pages><style face="normal" font="default" size="100%">389-390</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><notes><style face="normal" font="default" size="100%">cited By 0</style></notes></record></records></xml>