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Biochemical and molecular diagnosis of tyrosinemia type I with two novel FAH mutations in a Hong Kong chinese patient: Recommendation for expanded newborn screening in Hong Kong

✍ Scribed by Mak, Chloe Miu; Lam, Ching-wan; Chim, Stella; Siu, Tak-shing; Ng, King-fai; Tam, Sidney


Book ID
122059237
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
694 KB
Volume
46
Category
Article
ISSN
0009-9120

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