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A GPHN point mutation leading to molybdenum cofactor deficiency
Author(s) -
Reiss J,
Lenz U,
AquavivaBourdain C,
JoriotChekaf S,
MentionMulliez K,
HolderEspinasse M
Publication year - 2011
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2011.01709.x
Subject(s) - library science , humanities , philosophy , computer science
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