First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation

[11] Modifier genes convert "simple" Mendelian disorders to complex traits [J]. MOLECULAR GENETICS AND METABOLISM, 2000, 71 (1-2) : 43 - 50

[12] Differential developmental and tissue-specific regulation of expression of the genes encoding three members of the flavin-containing monooxygenase family of man, FMO1, FM03 and FM04 [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 235 (03): : 683 - 689

[13] The Currarino triad: the variable expression [J]. JOURNAL OF PEDIATRIC SURGERY, 2005, 40 (08) : 1238 - 1242

[14] Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome [J]. CLINICAL CHEMISTRY, 2006, 52 (01) : 46 - 52

[15] MNX1 (HLXB9) mutations in Currarino patients [J]. JOURNAL OF PEDIATRIC SURGERY, 2009, 44 (10) : 1892 - 1898

[16] HARRISON KA, 1994, J BIOL CHEM, V269, P19968

[17] Hughes James N, 2013, Methods Mol Biol, V1017, P135, DOI 10.1007/978-1-62703-438-8_10

[18] Epidermoid Cyst Inside Anterior Sacral Meningocele in an Adult Patient of Currarino Syndrome Manifesting with Meningitis [J]. TURKISH NEUROSURGERY, 2012, 22 (05) : 659 - 661

[19] Spectrum of mutations and genotype -: phenotype analysis in Currarino syndrome [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (08) : 599 - 605

[20] Discovery of novel flavin-containing monooxygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants [J]. MOLECULAR PHARMACOLOGY, 2005, 68 (02) : 383 - 392

[11] Modifier genes convert "simple" Mendelian disorders to complex traits [J]. MOLECULAR GENETICS AND METABOLISM, 2000, 71 (1-2) : 43 - 50

[12] Differential developmental and tissue-specific regulation of expression of the genes encoding three members of the flavin-containing monooxygenase family of man, FMO1, FM03 and FM04 [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 235 (03): : 683 - 689

[13] The Currarino triad: the variable expression [J]. JOURNAL OF PEDIATRIC SURGERY, 2005, 40 (08) : 1238 - 1242

[14] Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome [J]. CLINICAL CHEMISTRY, 2006, 52 (01) : 46 - 52

[15] MNX1 (HLXB9) mutations in Currarino patients [J]. JOURNAL OF PEDIATRIC SURGERY, 2009, 44 (10) : 1892 - 1898

[16] HARRISON KA, 1994, J BIOL CHEM, V269, P19968

[17] Hughes James N, 2013, Methods Mol Biol, V1017, P135, DOI 10.1007/978-1-62703-438-8_10

[18] Epidermoid Cyst Inside Anterior Sacral Meningocele in an Adult Patient of Currarino Syndrome Manifesting with Meningitis [J]. TURKISH NEUROSURGERY, 2012, 22 (05) : 659 - 661

[19] Spectrum of mutations and genotype -: phenotype analysis in Currarino syndrome [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (08) : 599 - 605

[20] Discovery of novel flavin-containing monooxygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants [J]. MOLECULAR PHARMACOLOGY, 2005, 68 (02) : 383 - 392